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You searched for subject:(Prenatal Diagnosis). Showing records 1 – 30 of 161 total matches.

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University of Zambia

1. Banda, Isaac. Factors associated with late antenatal care attendance in selected rural and urban communities of the copperbelt province,Zambia .

Degree: 2012, University of Zambia

 Background: Despite antenatal care services being provided free of charge or sometimes at a minimal cost in Zambia, only 19% of women attend antenatal care… (more)

Subjects/Keywords: Prenatal Diagnosis; Prenatal care

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APA (6th Edition):

Banda, I. (2012). Factors associated with late antenatal care attendance in selected rural and urban communities of the copperbelt province,Zambia . (Thesis). University of Zambia. Retrieved from http://hdl.handle.net/123456789/1830

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Banda, Isaac. “Factors associated with late antenatal care attendance in selected rural and urban communities of the copperbelt province,Zambia .” 2012. Thesis, University of Zambia. Accessed October 13, 2019. http://hdl.handle.net/123456789/1830.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Banda, Isaac. “Factors associated with late antenatal care attendance in selected rural and urban communities of the copperbelt province,Zambia .” 2012. Web. 13 Oct 2019.

Vancouver:

Banda I. Factors associated with late antenatal care attendance in selected rural and urban communities of the copperbelt province,Zambia . [Internet] [Thesis]. University of Zambia; 2012. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/123456789/1830.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Banda I. Factors associated with late antenatal care attendance in selected rural and urban communities of the copperbelt province,Zambia . [Thesis]. University of Zambia; 2012. Available from: http://hdl.handle.net/123456789/1830

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

2. 許佩華; Hui, Pui-wah. Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction.

Degree: Doctor of Medicine, 2014, University of Hong Kong

 Assisted reproduction technology is increasingly used for treatment of couples with subfertility. These women are usually of more advanced maternal age and carry a higher… (more)

Subjects/Keywords: Prenatal diagnosis; Down syndrome

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APA (6th Edition):

許佩華; Hui, P. (2014). Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction. (Doctoral Dissertation). University of Hong Kong. Retrieved from Hui, P. [許佩華]. (2014). Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5361008 ; http://dx.doi.org/10.5353/th_b5361008 ; http://hdl.handle.net/10722/208518

Chicago Manual of Style (16th Edition):

許佩華; Hui, Pui-wah. “Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed October 13, 2019. Hui, P. [許佩華]. (2014). Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5361008 ; http://dx.doi.org/10.5353/th_b5361008 ; http://hdl.handle.net/10722/208518.

MLA Handbook (7th Edition):

許佩華; Hui, Pui-wah. “Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction.” 2014. Web. 13 Oct 2019.

Vancouver:

許佩華; Hui P. Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2019 Oct 13]. Available from: Hui, P. [許佩華]. (2014). Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5361008 ; http://dx.doi.org/10.5353/th_b5361008 ; http://hdl.handle.net/10722/208518.

Council of Science Editors:

許佩華; Hui P. Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Hui, P. [許佩華]. (2014). Markers of Down syndrome and fetal growth profile in pregnancies conceived with assisted reproduction. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5361008 ; http://dx.doi.org/10.5353/th_b5361008 ; http://hdl.handle.net/10722/208518


University of Hong Kong

3. Leung, Wing-cheong. Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis.

Degree: Doctor of Medicine, 2010, University of Hong Kong

published_or_final_version

Medicine

Master

Doctor of Medicine

Subjects/Keywords: Prenatal diagnosis.

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APA (6th Edition):

Leung, W. (2010). Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis. (Doctoral Dissertation). University of Hong Kong. Retrieved from Leung, W. [梁永昌]. (2010). Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4520553 ; http://dx.doi.org/10.5353/th_b4520553 ; http://hdl.handle.net/10722/132149

Chicago Manual of Style (16th Edition):

Leung, Wing-cheong. “Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis.” 2010. Doctoral Dissertation, University of Hong Kong. Accessed October 13, 2019. Leung, W. [梁永昌]. (2010). Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4520553 ; http://dx.doi.org/10.5353/th_b4520553 ; http://hdl.handle.net/10722/132149.

MLA Handbook (7th Edition):

Leung, Wing-cheong. “Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis.” 2010. Web. 13 Oct 2019.

Vancouver:

Leung W. Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis. [Internet] [Doctoral dissertation]. University of Hong Kong; 2010. [cited 2019 Oct 13]. Available from: Leung, W. [梁永昌]. (2010). Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4520553 ; http://dx.doi.org/10.5353/th_b4520553 ; http://hdl.handle.net/10722/132149.

Council of Science Editors:

Leung W. Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis. [Doctoral Dissertation]. University of Hong Kong; 2010. Available from: Leung, W. [梁永昌]. (2010). Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4520553 ; http://dx.doi.org/10.5353/th_b4520553 ; http://hdl.handle.net/10722/132149


University of New South Wales

4. Sinnerbrink , Ingrid Brigitte. The health and developmental outcomes of children with a de novo apparently balanced chromosome rearrangement identified at prenatal diagnosis and the associated psychosocial impact on parents.

Degree: Women's & Children's Health, 2011, University of New South Wales

 The prenatal diagnosis of a de novo apparently balanced chromosomal rearrangement (ABCR), poses a geneticcounselling challenge because (a) there is a paucity of long-term health… (more)

Subjects/Keywords: Outcomes; Chromosome abnormalities; Prenatal diagnosis

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APA (6th Edition):

Sinnerbrink , I. B. (2011). The health and developmental outcomes of children with a de novo apparently balanced chromosome rearrangement identified at prenatal diagnosis and the associated psychosocial impact on parents. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50890 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9784/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Sinnerbrink , Ingrid Brigitte. “The health and developmental outcomes of children with a de novo apparently balanced chromosome rearrangement identified at prenatal diagnosis and the associated psychosocial impact on parents.” 2011. Masters Thesis, University of New South Wales. Accessed October 13, 2019. http://handle.unsw.edu.au/1959.4/50890 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9784/SOURCE02?view=true.

MLA Handbook (7th Edition):

Sinnerbrink , Ingrid Brigitte. “The health and developmental outcomes of children with a de novo apparently balanced chromosome rearrangement identified at prenatal diagnosis and the associated psychosocial impact on parents.” 2011. Web. 13 Oct 2019.

Vancouver:

Sinnerbrink IB. The health and developmental outcomes of children with a de novo apparently balanced chromosome rearrangement identified at prenatal diagnosis and the associated psychosocial impact on parents. [Internet] [Masters thesis]. University of New South Wales; 2011. [cited 2019 Oct 13]. Available from: http://handle.unsw.edu.au/1959.4/50890 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9784/SOURCE02?view=true.

Council of Science Editors:

Sinnerbrink IB. The health and developmental outcomes of children with a de novo apparently balanced chromosome rearrangement identified at prenatal diagnosis and the associated psychosocial impact on parents. [Masters Thesis]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/50890 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9784/SOURCE02?view=true


University of Hong Kong

5. 蘇寶琳; So, Po-lam. Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling.

Degree: Master of Medical Sciences, 2015, University of Hong Kong

 Objectives With advancement of technology in genetic testing and widespread use of prenatal diagnosis, the prenatal detection of sex chromosome aneuploidies (SCA) is often unavoidable.… (more)

Subjects/Keywords: Genetic disorders; Prenatal diagnosis; Genetic counseling

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APA (6th Edition):

蘇寶琳; So, P. (2015). Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. (Masters Thesis). University of Hong Kong. Retrieved from So, P. [蘇寶琳]. (2015). Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5734121 ; http://hdl.handle.net/10722/225095

Chicago Manual of Style (16th Edition):

蘇寶琳; So, Po-lam. “Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling.” 2015. Masters Thesis, University of Hong Kong. Accessed October 13, 2019. So, P. [蘇寶琳]. (2015). Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5734121 ; http://hdl.handle.net/10722/225095.

MLA Handbook (7th Edition):

蘇寶琳; So, Po-lam. “Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling.” 2015. Web. 13 Oct 2019.

Vancouver:

蘇寶琳; So P. Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Oct 13]. Available from: So, P. [蘇寶琳]. (2015). Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5734121 ; http://hdl.handle.net/10722/225095.

Council of Science Editors:

蘇寶琳; So P. Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. [Masters Thesis]. University of Hong Kong; 2015. Available from: So, P. [蘇寶琳]. (2015). Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5734121 ; http://hdl.handle.net/10722/225095


University of Hong Kong

6. 鄭靜恩; Cheng, Ching-yan, Serene. Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection.

Degree: Master of Medical Sciences, 2017, University of Hong Kong

Aneuploidy is one of the known major causes of miscarriage and congenital birth defects. It refers to chromosomal abnormality with chromosome number being different from… (more)

Subjects/Keywords: Genetic counseling; Prenatal diagnosis; Genetic disorders

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APA (6th Edition):

鄭靜恩; Cheng, Ching-yan, S. (2017). Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/251327

Chicago Manual of Style (16th Edition):

鄭靜恩; Cheng, Ching-yan, Serene. “Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection.” 2017. Masters Thesis, University of Hong Kong. Accessed October 13, 2019. http://hdl.handle.net/10722/251327.

MLA Handbook (7th Edition):

鄭靜恩; Cheng, Ching-yan, Serene. “Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection.” 2017. Web. 13 Oct 2019.

Vancouver:

鄭靜恩; Cheng, Ching-yan S. Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection. [Internet] [Masters thesis]. University of Hong Kong; 2017. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10722/251327.

Council of Science Editors:

鄭靜恩; Cheng, Ching-yan S. Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection. [Masters Thesis]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/251327


University of Hong Kong

7. Yau, Hoi-ying, Alice. Risk communication in prenatal screening for Down syndrome: a discourse analytic study of patients'risk talk.

Degree: M. Phil., 2012, University of Hong Kong

Risk is a crucial concept in healthcare communication. This is attested to by a large body of research on risk communication in psychology, sociology, and,… (more)

Subjects/Keywords: Prenatal diagnosis.; Discourse analysis.; Down syndrome.

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APA (6th Edition):

Yau, Hoi-ying, A. (2012). Risk communication in prenatal screening for Down syndrome: a discourse analytic study of patients'risk talk. (Masters Thesis). University of Hong Kong. Retrieved from Yau, H. A. [邱凱盈]. (2012). Risk communication in prenatal screening for Down syndrome : a discourse analytic study of patients' risk talk. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4807979 ; http://dx.doi.org/10.5353/th_b4807979 ; http://hdl.handle.net/10722/161574

Chicago Manual of Style (16th Edition):

Yau, Hoi-ying, Alice. “Risk communication in prenatal screening for Down syndrome: a discourse analytic study of patients'risk talk.” 2012. Masters Thesis, University of Hong Kong. Accessed October 13, 2019. Yau, H. A. [邱凱盈]. (2012). Risk communication in prenatal screening for Down syndrome : a discourse analytic study of patients' risk talk. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4807979 ; http://dx.doi.org/10.5353/th_b4807979 ; http://hdl.handle.net/10722/161574.

MLA Handbook (7th Edition):

Yau, Hoi-ying, Alice. “Risk communication in prenatal screening for Down syndrome: a discourse analytic study of patients'risk talk.” 2012. Web. 13 Oct 2019.

Vancouver:

Yau, Hoi-ying A. Risk communication in prenatal screening for Down syndrome: a discourse analytic study of patients'risk talk. [Internet] [Masters thesis]. University of Hong Kong; 2012. [cited 2019 Oct 13]. Available from: Yau, H. A. [邱凱盈]. (2012). Risk communication in prenatal screening for Down syndrome : a discourse analytic study of patients' risk talk. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4807979 ; http://dx.doi.org/10.5353/th_b4807979 ; http://hdl.handle.net/10722/161574.

Council of Science Editors:

Yau, Hoi-ying A. Risk communication in prenatal screening for Down syndrome: a discourse analytic study of patients'risk talk. [Masters Thesis]. University of Hong Kong; 2012. Available from: Yau, H. A. [邱凱盈]. (2012). Risk communication in prenatal screening for Down syndrome : a discourse analytic study of patients' risk talk. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4807979 ; http://dx.doi.org/10.5353/th_b4807979 ; http://hdl.handle.net/10722/161574


Case Western Reserve University

8. Smith, Marissa B. A Description of Genetic Counselors' Views and Current Practice with Regard to the Use of Array-CGH for Prenatal Diagnosis.

Degree: MSs, Genetic Counseling, 2009, Case Western Reserve University

 While experience with array comparative genomic hybridization (array-CGH) in the pediatric setting is extensive, its use for prenatal diagnosis is limited. A descriptive web-based survey… (more)

Subjects/Keywords: Genetics; genetic counseling; array-CGH; prenatal diagnosis

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APA (6th Edition):

Smith, M. B. (2009). A Description of Genetic Counselors' Views and Current Practice with Regard to the Use of Array-CGH for Prenatal Diagnosis. (Masters Thesis). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1246977726

Chicago Manual of Style (16th Edition):

Smith, Marissa B. “A Description of Genetic Counselors' Views and Current Practice with Regard to the Use of Array-CGH for Prenatal Diagnosis.” 2009. Masters Thesis, Case Western Reserve University. Accessed October 13, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1246977726.

MLA Handbook (7th Edition):

Smith, Marissa B. “A Description of Genetic Counselors' Views and Current Practice with Regard to the Use of Array-CGH for Prenatal Diagnosis.” 2009. Web. 13 Oct 2019.

Vancouver:

Smith MB. A Description of Genetic Counselors' Views and Current Practice with Regard to the Use of Array-CGH for Prenatal Diagnosis. [Internet] [Masters thesis]. Case Western Reserve University; 2009. [cited 2019 Oct 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1246977726.

Council of Science Editors:

Smith MB. A Description of Genetic Counselors' Views and Current Practice with Regard to the Use of Array-CGH for Prenatal Diagnosis. [Masters Thesis]. Case Western Reserve University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1246977726


Univerzitet u Beogradu

9. Radojković, Dragica, 1959-. Prenatalna dijagnostika cistične fibroze primenom metoda rekombinantne DNK.

Degree: Biološki fakultet, 2018, Univerzitet u Beogradu

Биологија / молекуларна биологија ; Biology / molecular biology

Cistična fibroza je najčešće autozomno recesivno oboljenje, koje se u opulaciji belaca javlja saučestalošću od 1/2000… (more)

Subjects/Keywords: cystic fibrosis; prenatal diagnosis; mutation analysis

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APA (6th Edition):

Radojković, Dragica, 1. (2018). Prenatalna dijagnostika cistične fibroze primenom metoda rekombinantne DNK. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:18973/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Radojković, Dragica, 1959-. “Prenatalna dijagnostika cistične fibroze primenom metoda rekombinantne DNK.” 2018. Thesis, Univerzitet u Beogradu. Accessed October 13, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:18973/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Radojković, Dragica, 1959-. “Prenatalna dijagnostika cistične fibroze primenom metoda rekombinantne DNK.” 2018. Web. 13 Oct 2019.

Vancouver:

Radojković, Dragica 1. Prenatalna dijagnostika cistične fibroze primenom metoda rekombinantne DNK. [Internet] [Thesis]. Univerzitet u Beogradu; 2018. [cited 2019 Oct 13]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:18973/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Radojković, Dragica 1. Prenatalna dijagnostika cistične fibroze primenom metoda rekombinantne DNK. [Thesis]. Univerzitet u Beogradu; 2018. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:18973/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Stellenbosch University

10. Scott, Chantelle Jennifer. Understanding decision-making regarding prenatal diagnostic testing for down syndrome and termination of pregnancy: an interpretive phenomenological study.

Degree: PhD, Biomedical Sciences, 2018, Stellenbosch University

 ENGLISH ABSTRACT: Pregnant women or couples who screen high risk for a baby with Down syndrome (DS) are faced with having to make life changing… (more)

Subjects/Keywords: Prenatal care; Down syndrome; Prenatal diagnosis; Pregnancy termination; UCTD

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APA (6th Edition):

Scott, C. J. (2018). Understanding decision-making regarding prenatal diagnostic testing for down syndrome and termination of pregnancy: an interpretive phenomenological study. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/103453

Chicago Manual of Style (16th Edition):

Scott, Chantelle Jennifer. “Understanding decision-making regarding prenatal diagnostic testing for down syndrome and termination of pregnancy: an interpretive phenomenological study.” 2018. Doctoral Dissertation, Stellenbosch University. Accessed October 13, 2019. http://hdl.handle.net/10019.1/103453.

MLA Handbook (7th Edition):

Scott, Chantelle Jennifer. “Understanding decision-making regarding prenatal diagnostic testing for down syndrome and termination of pregnancy: an interpretive phenomenological study.” 2018. Web. 13 Oct 2019.

Vancouver:

Scott CJ. Understanding decision-making regarding prenatal diagnostic testing for down syndrome and termination of pregnancy: an interpretive phenomenological study. [Internet] [Doctoral dissertation]. Stellenbosch University; 2018. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10019.1/103453.

Council of Science Editors:

Scott CJ. Understanding decision-making regarding prenatal diagnostic testing for down syndrome and termination of pregnancy: an interpretive phenomenological study. [Doctoral Dissertation]. Stellenbosch University; 2018. Available from: http://hdl.handle.net/10019.1/103453


Brandeis University

11. Maliszewski, Kristen. An Assessment of Genetic Counselors’ Opinions on How Non-Invasive Prenatal Diagnosis May Impact Genetic Counseling Services.

Degree: 2010, Brandeis University

 Non-invasive prenatal diagnosis (NIPD) is a promising prenatal diagnostic technology that is currently being developed. The premise behind it is that fetal DNA can be… (more)

Subjects/Keywords: Genetic counseling; Non-invasive prenatal diagnosis; Prenatal testing

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APA (6th Edition):

Maliszewski, K. (2010). An Assessment of Genetic Counselors’ Opinions on How Non-Invasive Prenatal Diagnosis May Impact Genetic Counseling Services. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/24065

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Maliszewski, Kristen. “An Assessment of Genetic Counselors’ Opinions on How Non-Invasive Prenatal Diagnosis May Impact Genetic Counseling Services.” 2010. Thesis, Brandeis University. Accessed October 13, 2019. http://hdl.handle.net/10192/24065.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Maliszewski, Kristen. “An Assessment of Genetic Counselors’ Opinions on How Non-Invasive Prenatal Diagnosis May Impact Genetic Counseling Services.” 2010. Web. 13 Oct 2019.

Vancouver:

Maliszewski K. An Assessment of Genetic Counselors’ Opinions on How Non-Invasive Prenatal Diagnosis May Impact Genetic Counseling Services. [Internet] [Thesis]. Brandeis University; 2010. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10192/24065.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Maliszewski K. An Assessment of Genetic Counselors’ Opinions on How Non-Invasive Prenatal Diagnosis May Impact Genetic Counseling Services. [Thesis]. Brandeis University; 2010. Available from: http://hdl.handle.net/10192/24065

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

12. Wong, Hoi-hei, Vera. Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis.

Degree: M. Phil., 2015, University of Hong Kong

There has been an increase in rates of chromosomal abnormalities in newborns as a result of reproductive aging. For the past decades, a lot of… (more)

Subjects/Keywords: Keratin; HLA histocompatibility antigens; Fetus - Abnormalities - Diagnosis; Prenatal diagnosis

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APA (6th Edition):

Wong, Hoi-hei, V. (2015). Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis. (Masters Thesis). University of Hong Kong. Retrieved from Wong, H. V. [王愷曦]. (2015). Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5388026 ; http://dx.doi.org/10.5353/th_b5388026 ; http://hdl.handle.net/10722/208587

Chicago Manual of Style (16th Edition):

Wong, Hoi-hei, Vera. “Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis.” 2015. Masters Thesis, University of Hong Kong. Accessed October 13, 2019. Wong, H. V. [王愷曦]. (2015). Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5388026 ; http://dx.doi.org/10.5353/th_b5388026 ; http://hdl.handle.net/10722/208587.

MLA Handbook (7th Edition):

Wong, Hoi-hei, Vera. “Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis.” 2015. Web. 13 Oct 2019.

Vancouver:

Wong, Hoi-hei V. Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Oct 13]. Available from: Wong, H. V. [王愷曦]. (2015). Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5388026 ; http://dx.doi.org/10.5353/th_b5388026 ; http://hdl.handle.net/10722/208587.

Council of Science Editors:

Wong, Hoi-hei V. Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis. [Masters Thesis]. University of Hong Kong; 2015. Available from: Wong, H. V. [王愷曦]. (2015). Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5388026 ; http://dx.doi.org/10.5353/th_b5388026 ; http://hdl.handle.net/10722/208587


University of Hong Kong

13. 朱繼光; Chu, Kai-kwong, Gino. Education, information and guidance in genetic counseling of prenatal diagnostic tests for chromosomal abnormalities.

Degree: Master of Medical Sciences, 2015, University of Hong Kong

 The study is conceived and designed with its goals to find out what elements matter most when people have to make decision about (i) whether… (more)

Subjects/Keywords: Genetic counseling; Prenatal diagnosis; Human chromosome abnormalities - Diagnosis

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APA (6th Edition):

朱繼光; Chu, Kai-kwong, G. (2015). Education, information and guidance in genetic counseling of prenatal diagnostic tests for chromosomal abnormalities. (Masters Thesis). University of Hong Kong. Retrieved from Chu, K. G. [朱繼光]. (2015). Education, information and guidance in genetic counseling of prenatal diagnostic tests for chromosomal abnormalities. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5623505 ; http://hdl.handle.net/10722/221474

Chicago Manual of Style (16th Edition):

朱繼光; Chu, Kai-kwong, Gino. “Education, information and guidance in genetic counseling of prenatal diagnostic tests for chromosomal abnormalities.” 2015. Masters Thesis, University of Hong Kong. Accessed October 13, 2019. Chu, K. G. [朱繼光]. (2015). Education, information and guidance in genetic counseling of prenatal diagnostic tests for chromosomal abnormalities. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5623505 ; http://hdl.handle.net/10722/221474.

MLA Handbook (7th Edition):

朱繼光; Chu, Kai-kwong, Gino. “Education, information and guidance in genetic counseling of prenatal diagnostic tests for chromosomal abnormalities.” 2015. Web. 13 Oct 2019.

Vancouver:

朱繼光; Chu, Kai-kwong G. Education, information and guidance in genetic counseling of prenatal diagnostic tests for chromosomal abnormalities. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Oct 13]. Available from: Chu, K. G. [朱繼光]. (2015). Education, information and guidance in genetic counseling of prenatal diagnostic tests for chromosomal abnormalities. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5623505 ; http://hdl.handle.net/10722/221474.

Council of Science Editors:

朱繼光; Chu, Kai-kwong G. Education, information and guidance in genetic counseling of prenatal diagnostic tests for chromosomal abnormalities. [Masters Thesis]. University of Hong Kong; 2015. Available from: Chu, K. G. [朱繼光]. (2015). Education, information and guidance in genetic counseling of prenatal diagnostic tests for chromosomal abnormalities. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5623505 ; http://hdl.handle.net/10722/221474

14. Ramos, Juliana Limeira de Araujo Moura. Caracterização sócio demográfica e resultados perinatais das gestações com diagnóstico ultra-sonográfico de malformação fetal maior avaliadas em centro de referência.

Degree: Mestrado, Obstetrícia e Ginecologia, 2008, University of São Paulo

Com o objetivo de caracterizar, do ponto de vista sócio-demográfico, e obter a evolução pós-natal, das gestantes com diagnóstico ultra-sonográfico pré-natal de malformação fetal maior,… (more)

Subjects/Keywords: Anormalidades congênitas; Congenital abnormalities; Diagnóstico pré-natal; Prenatal diagnosis; Prenatal ultrasonography; Ultra-sonografia pré-natal

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APA (6th Edition):

Ramos, J. L. d. A. M. (2008). Caracterização sócio demográfica e resultados perinatais das gestações com diagnóstico ultra-sonográfico de malformação fetal maior avaliadas em centro de referência. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5139/tde-13012009-113705/ ;

Chicago Manual of Style (16th Edition):

Ramos, Juliana Limeira de Araujo Moura. “Caracterização sócio demográfica e resultados perinatais das gestações com diagnóstico ultra-sonográfico de malformação fetal maior avaliadas em centro de referência.” 2008. Masters Thesis, University of São Paulo. Accessed October 13, 2019. http://www.teses.usp.br/teses/disponiveis/5/5139/tde-13012009-113705/ ;.

MLA Handbook (7th Edition):

Ramos, Juliana Limeira de Araujo Moura. “Caracterização sócio demográfica e resultados perinatais das gestações com diagnóstico ultra-sonográfico de malformação fetal maior avaliadas em centro de referência.” 2008. Web. 13 Oct 2019.

Vancouver:

Ramos JLdAM. Caracterização sócio demográfica e resultados perinatais das gestações com diagnóstico ultra-sonográfico de malformação fetal maior avaliadas em centro de referência. [Internet] [Masters thesis]. University of São Paulo; 2008. [cited 2019 Oct 13]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5139/tde-13012009-113705/ ;.

Council of Science Editors:

Ramos JLdAM. Caracterização sócio demográfica e resultados perinatais das gestações com diagnóstico ultra-sonográfico de malformação fetal maior avaliadas em centro de referência. [Masters Thesis]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/5/5139/tde-13012009-113705/ ;


Texas Medical Center

15. Davis, Jessica. ATTITUDES TOWARD AND UTILIZATION OF NON-INVASIVE PRENATAL TESTING FOR CHROMOSOME ANEUPLOIDY AMONG OB/GYNS.

Degree: MS, 2013, Texas Medical Center

Prenatal diagnosis is traditionally made via invasive procedures such as amniocentesis and chorionic villus sampling (CVS). However, both procedures carry a risk of complications,… (more)

Subjects/Keywords: NIPT; prenatal screening; attitudes; utilization; obstetrics; prenatal diagnosis; Medicine and Health Sciences; Obstetrics and Gynecology

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APA (6th Edition):

Davis, J. (2013). ATTITUDES TOWARD AND UTILIZATION OF NON-INVASIVE PRENATAL TESTING FOR CHROMOSOME ANEUPLOIDY AMONG OB/GYNS. (Masters Thesis). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/352

Chicago Manual of Style (16th Edition):

Davis, Jessica. “ATTITUDES TOWARD AND UTILIZATION OF NON-INVASIVE PRENATAL TESTING FOR CHROMOSOME ANEUPLOIDY AMONG OB/GYNS.” 2013. Masters Thesis, Texas Medical Center. Accessed October 13, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/352.

MLA Handbook (7th Edition):

Davis, Jessica. “ATTITUDES TOWARD AND UTILIZATION OF NON-INVASIVE PRENATAL TESTING FOR CHROMOSOME ANEUPLOIDY AMONG OB/GYNS.” 2013. Web. 13 Oct 2019.

Vancouver:

Davis J. ATTITUDES TOWARD AND UTILIZATION OF NON-INVASIVE PRENATAL TESTING FOR CHROMOSOME ANEUPLOIDY AMONG OB/GYNS. [Internet] [Masters thesis]. Texas Medical Center; 2013. [cited 2019 Oct 13]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/352.

Council of Science Editors:

Davis J. ATTITUDES TOWARD AND UTILIZATION OF NON-INVASIVE PRENATAL TESTING FOR CHROMOSOME ANEUPLOIDY AMONG OB/GYNS. [Masters Thesis]. Texas Medical Center; 2013. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/352

16. Ordóñez Torra, Elena. DNA fetal libre en plasma materno: desarrollo de nuevos métodos de análisis y aplicación clínica en diagnóstico prenatal no invasivo.

Degree: Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia, 2016, Universitat Autònoma de Barcelona

 The discover in 1997 of the presence of cell free fetal DNA in maternal plasma opened new perspectives in prenatal diagnosis, allowing accessing fetal genetic… (more)

Subjects/Keywords: Diagnòstic prenatal; Diagnóstico prenatal; Prenatal diagnosis; No invasiu; No invasivo; Non invasive; DNA fetal; Fetal DNA; Ciències Experimentals; 577

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APA (6th Edition):

Ordóñez Torra, E. (2016). DNA fetal libre en plasma materno: desarrollo de nuevos métodos de análisis y aplicación clínica en diagnóstico prenatal no invasivo. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/401105

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ordóñez Torra, Elena. “DNA fetal libre en plasma materno: desarrollo de nuevos métodos de análisis y aplicación clínica en diagnóstico prenatal no invasivo.” 2016. Thesis, Universitat Autònoma de Barcelona. Accessed October 13, 2019. http://hdl.handle.net/10803/401105.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ordóñez Torra, Elena. “DNA fetal libre en plasma materno: desarrollo de nuevos métodos de análisis y aplicación clínica en diagnóstico prenatal no invasivo.” 2016. Web. 13 Oct 2019.

Vancouver:

Ordóñez Torra E. DNA fetal libre en plasma materno: desarrollo de nuevos métodos de análisis y aplicación clínica en diagnóstico prenatal no invasivo. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2016. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10803/401105.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ordóñez Torra E. DNA fetal libre en plasma materno: desarrollo de nuevos métodos de análisis y aplicación clínica en diagnóstico prenatal no invasivo. [Thesis]. Universitat Autònoma de Barcelona; 2016. Available from: http://hdl.handle.net/10803/401105

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universitat Autònoma de Barcelona

17. Maroto González, Anna. Nivell neurològic prenatal en fetus afectes de mielomeningocele sotmesos a cirurgia intraúter.

Degree: Departament de Pediatria, d'Obstetrícia i Ginecologia i de Medicina Preventiva, 2017, Universitat Autònoma de Barcelona

 Myelomeningocele (MMC) is a congenital malformation characterized by the extrusion of the spinal cord as a result of a lack of fusion of vertebral arches… (more)

Subjects/Keywords: Mielomeningocele; Cirurgia fetal; Cirugía fetal; Fetal surgery; Diagnòstic prenatal; Diagnóstico prenatal; Prenatal diagnosis; Ciències de la Salut; 618

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APA (6th Edition):

Maroto González, A. (2017). Nivell neurològic prenatal en fetus afectes de mielomeningocele sotmesos a cirurgia intraúter. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/454873

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Maroto González, Anna. “Nivell neurològic prenatal en fetus afectes de mielomeningocele sotmesos a cirurgia intraúter.” 2017. Thesis, Universitat Autònoma de Barcelona. Accessed October 13, 2019. http://hdl.handle.net/10803/454873.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Maroto González, Anna. “Nivell neurològic prenatal en fetus afectes de mielomeningocele sotmesos a cirurgia intraúter.” 2017. Web. 13 Oct 2019.

Vancouver:

Maroto González A. Nivell neurològic prenatal en fetus afectes de mielomeningocele sotmesos a cirurgia intraúter. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2017. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10803/454873.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Maroto González A. Nivell neurològic prenatal en fetus afectes de mielomeningocele sotmesos a cirurgia intraúter. [Thesis]. Universitat Autònoma de Barcelona; 2017. Available from: http://hdl.handle.net/10803/454873

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Gothenburg / Göteborgs Universitet

18. Wahlström, Jan, 1939-. Prenatal kromosombestämning : undersökning av celler ur fostervatten från gravida kvinnor 35 år eller äldre = Prenatal analysis of the chromosome constitution : examination of cells from the amniotic fluid of pregnant women aged 35 and over.

Degree: 1972, University of Gothenburg / Göteborgs Universitet

Subjects/Keywords: Biologi Genetik Chromosomes; Prenatal diagnosis

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APA (6th Edition):

Wahlström, Jan, 1. (1972). Prenatal kromosombestämning : undersökning av celler ur fostervatten från gravida kvinnor 35 år eller äldre = Prenatal analysis of the chromosome constitution : examination of cells from the amniotic fluid of pregnant women aged 35 and over. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/14749

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wahlström, Jan, 1939-. “Prenatal kromosombestämning : undersökning av celler ur fostervatten från gravida kvinnor 35 år eller äldre = Prenatal analysis of the chromosome constitution : examination of cells from the amniotic fluid of pregnant women aged 35 and over.” 1972. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 13, 2019. http://hdl.handle.net/2077/14749.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wahlström, Jan, 1939-. “Prenatal kromosombestämning : undersökning av celler ur fostervatten från gravida kvinnor 35 år eller äldre = Prenatal analysis of the chromosome constitution : examination of cells from the amniotic fluid of pregnant women aged 35 and over.” 1972. Web. 13 Oct 2019.

Vancouver:

Wahlström, Jan 1. Prenatal kromosombestämning : undersökning av celler ur fostervatten från gravida kvinnor 35 år eller äldre = Prenatal analysis of the chromosome constitution : examination of cells from the amniotic fluid of pregnant women aged 35 and over. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 1972. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/2077/14749.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wahlström, Jan 1. Prenatal kromosombestämning : undersökning av celler ur fostervatten från gravida kvinnor 35 år eller äldre = Prenatal analysis of the chromosome constitution : examination of cells from the amniotic fluid of pregnant women aged 35 and over. [Thesis]. University of Gothenburg / Göteborgs Universitet; 1972. Available from: http://hdl.handle.net/2077/14749

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Nelson Mandela Metropolitan University

19. Pienaar, Nadine. The experiences of pregnant teenagers as related to ante-natal care.

Degree: Faculty of Health Sciences, 2011, Nelson Mandela Metropolitan University

 The experiences of pregnant teenagers as related to ante-natal care were researched. The primary objective of the study was to explore and describe the experiences… (more)

Subjects/Keywords: Pregnant teenagers  – South Africa  – Nelson Mandela Metropolitan Municpality; Prenatal diagnosis

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APA (6th Edition):

Pienaar, N. (2011). The experiences of pregnant teenagers as related to ante-natal care. (Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/1321

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Pienaar, Nadine. “The experiences of pregnant teenagers as related to ante-natal care.” 2011. Thesis, Nelson Mandela Metropolitan University. Accessed October 13, 2019. http://hdl.handle.net/10948/1321.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Pienaar, Nadine. “The experiences of pregnant teenagers as related to ante-natal care.” 2011. Web. 13 Oct 2019.

Vancouver:

Pienaar N. The experiences of pregnant teenagers as related to ante-natal care. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2011. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10948/1321.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Pienaar N. The experiences of pregnant teenagers as related to ante-natal care. [Thesis]. Nelson Mandela Metropolitan University; 2011. Available from: http://hdl.handle.net/10948/1321

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

20. 許佩華.; Hui, Pui-wah. Nuchal translucency in pregnancies conceived after assisted reproduction technology.

Degree: Master of Medical Sciences, 2003, University of Hong Kong

published_or_final_version

Medical Sciences

Master

Master of Medical Sciences

Subjects/Keywords: Prenatal diagnosis.; Down syndrome.

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APA (6th Edition):

許佩華.; Hui, P. (2003). Nuchal translucency in pregnancies conceived after assisted reproduction technology. (Masters Thesis). University of Hong Kong. Retrieved from Hui, P. [許佩華]. (2003). Nuchal translucency in pregnancies conceived after assisted reproduction technology. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197104 ; http://dx.doi.org/10.5353/th_b3197104 ; http://hdl.handle.net/10722/51968

Chicago Manual of Style (16th Edition):

許佩華.; Hui, Pui-wah. “Nuchal translucency in pregnancies conceived after assisted reproduction technology.” 2003. Masters Thesis, University of Hong Kong. Accessed October 13, 2019. Hui, P. [許佩華]. (2003). Nuchal translucency in pregnancies conceived after assisted reproduction technology. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197104 ; http://dx.doi.org/10.5353/th_b3197104 ; http://hdl.handle.net/10722/51968.

MLA Handbook (7th Edition):

許佩華.; Hui, Pui-wah. “Nuchal translucency in pregnancies conceived after assisted reproduction technology.” 2003. Web. 13 Oct 2019.

Vancouver:

許佩華.; Hui P. Nuchal translucency in pregnancies conceived after assisted reproduction technology. [Internet] [Masters thesis]. University of Hong Kong; 2003. [cited 2019 Oct 13]. Available from: Hui, P. [許佩華]. (2003). Nuchal translucency in pregnancies conceived after assisted reproduction technology. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197104 ; http://dx.doi.org/10.5353/th_b3197104 ; http://hdl.handle.net/10722/51968.

Council of Science Editors:

許佩華.; Hui P. Nuchal translucency in pregnancies conceived after assisted reproduction technology. [Masters Thesis]. University of Hong Kong; 2003. Available from: Hui, P. [許佩華]. (2003). Nuchal translucency in pregnancies conceived after assisted reproduction technology. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197104 ; http://dx.doi.org/10.5353/th_b3197104 ; http://hdl.handle.net/10722/51968


Montana Tech

21. Shors, Benjamin J. Notes from the ultrasound| A survey of prenatal testing in Montana.

Degree: MA, 2000, Montana Tech

Subjects/Keywords: Prenatal diagnosis Montana; Journalism; Scientific

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APA (6th Edition):

Shors, B. J. (2000). Notes from the ultrasound| A survey of prenatal testing in Montana. (Masters Thesis). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/3104

Chicago Manual of Style (16th Edition):

Shors, Benjamin J. “Notes from the ultrasound| A survey of prenatal testing in Montana.” 2000. Masters Thesis, Montana Tech. Accessed October 13, 2019. https://scholarworks.umt.edu/etd/3104.

MLA Handbook (7th Edition):

Shors, Benjamin J. “Notes from the ultrasound| A survey of prenatal testing in Montana.” 2000. Web. 13 Oct 2019.

Vancouver:

Shors BJ. Notes from the ultrasound| A survey of prenatal testing in Montana. [Internet] [Masters thesis]. Montana Tech; 2000. [cited 2019 Oct 13]. Available from: https://scholarworks.umt.edu/etd/3104.

Council of Science Editors:

Shors BJ. Notes from the ultrasound| A survey of prenatal testing in Montana. [Masters Thesis]. Montana Tech; 2000. Available from: https://scholarworks.umt.edu/etd/3104


Universidade Nova

22. Xavier, Maria José Pinto Barreira Rego de Sousa. Rastreio combinado do 1º trimestre e doenças autoimunes : Impacto das variaveis pré-analíticas na avaliação do risco.

Degree: 2014, Universidade Nova

 RESUMO: Contexto: As anomalias congénitas, com particular destaque para as neuploidias , afectam aproximadamente 2% dos recém-nascidos, constituindo causas frequentes de morbilidade e mortalidade. Actualmente,… (more)

Subjects/Keywords: Autoimmune Diseases - epidemiology; Pregnancy; Prenatal Diagnosis; Case Studies; Portugal; Medicina Laboratorial

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APA (6th Edition):

Xavier, M. J. P. B. R. d. S. (2014). Rastreio combinado do 1º trimestre e doenças autoimunes : Impacto das variaveis pré-analíticas na avaliação do risco. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/12156

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Xavier, Maria José Pinto Barreira Rego de Sousa. “Rastreio combinado do 1º trimestre e doenças autoimunes : Impacto das variaveis pré-analíticas na avaliação do risco.” 2014. Thesis, Universidade Nova. Accessed October 13, 2019. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/12156.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Xavier, Maria José Pinto Barreira Rego de Sousa. “Rastreio combinado do 1º trimestre e doenças autoimunes : Impacto das variaveis pré-analíticas na avaliação do risco.” 2014. Web. 13 Oct 2019.

Vancouver:

Xavier MJPBRdS. Rastreio combinado do 1º trimestre e doenças autoimunes : Impacto das variaveis pré-analíticas na avaliação do risco. [Internet] [Thesis]. Universidade Nova; 2014. [cited 2019 Oct 13]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/12156.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Xavier MJPBRdS. Rastreio combinado do 1º trimestre e doenças autoimunes : Impacto das variaveis pré-analíticas na avaliação do risco. [Thesis]. Universidade Nova; 2014. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/12156

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Univerzitet u Beogradu

23. Maksić, Jasmina, 1969-. Značaj određivanja statusa prenosioca kod Dišenove i Bekerove mišićne distrofije u populaciji Srbije.

Degree: Medicinski fakultet, 2019, Univerzitet u Beogradu

Medicina - Genetika / Medicine - Genetics

Distrofinopatije su bolesti koje nastaju kao posledica mutacija u genu za distrofin. Dišenova mišićna distrofija (DMD) predstavlja najteži… (more)

Subjects/Keywords: dystrophinopathies; mutations in DMD gene; female carrier; prenatal diagnosis

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Maksić, Jasmina, 1. (2019). Značaj određivanja statusa prenosioca kod Dišenove i Bekerove mišićne distrofije u populaciji Srbije. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:19145/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Maksić, Jasmina, 1969-. “Značaj određivanja statusa prenosioca kod Dišenove i Bekerove mišićne distrofije u populaciji Srbije.” 2019. Thesis, Univerzitet u Beogradu. Accessed October 13, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:19145/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Maksić, Jasmina, 1969-. “Značaj određivanja statusa prenosioca kod Dišenove i Bekerove mišićne distrofije u populaciji Srbije.” 2019. Web. 13 Oct 2019.

Vancouver:

Maksić, Jasmina 1. Značaj određivanja statusa prenosioca kod Dišenove i Bekerove mišićne distrofije u populaciji Srbije. [Internet] [Thesis]. Univerzitet u Beogradu; 2019. [cited 2019 Oct 13]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19145/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Maksić, Jasmina 1. Značaj određivanja statusa prenosioca kod Dišenove i Bekerove mišićne distrofije u populaciji Srbije. [Thesis]. Univerzitet u Beogradu; 2019. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19145/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of the Western Cape

24. Rassie, Candice. Optimisation of a microfluidic device for the pre-concentration and size separation of cell free foetal DNA from maternal plasma by capillary electrophoresis .

Degree: 2012, University of the Western Cape

 The discovery of cell free foetal DNA (cffDNA) in 1997 allows for the combination of accuracy as well as non-invasiveness for prenatal diagnosis. This non-invasive… (more)

Subjects/Keywords: Prenatal diagnosis; Cell free foetal DNA; Microfabrication; Fluorescence spectroscopy; Microfluidics

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APA (6th Edition):

Rassie, C. (2012). Optimisation of a microfluidic device for the pre-concentration and size separation of cell free foetal DNA from maternal plasma by capillary electrophoresis . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/4589

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rassie, Candice. “Optimisation of a microfluidic device for the pre-concentration and size separation of cell free foetal DNA from maternal plasma by capillary electrophoresis .” 2012. Thesis, University of the Western Cape. Accessed October 13, 2019. http://hdl.handle.net/11394/4589.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rassie, Candice. “Optimisation of a microfluidic device for the pre-concentration and size separation of cell free foetal DNA from maternal plasma by capillary electrophoresis .” 2012. Web. 13 Oct 2019.

Vancouver:

Rassie C. Optimisation of a microfluidic device for the pre-concentration and size separation of cell free foetal DNA from maternal plasma by capillary electrophoresis . [Internet] [Thesis]. University of the Western Cape; 2012. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/11394/4589.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rassie C. Optimisation of a microfluidic device for the pre-concentration and size separation of cell free foetal DNA from maternal plasma by capillary electrophoresis . [Thesis]. University of the Western Cape; 2012. Available from: http://hdl.handle.net/11394/4589

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Wayne State University

25. Fritz, Rani. Trophoblast Retrieval And Isolation From The Cervix (tric) For Non-Invasive Prenatal Genetic Diagnosis And Prediction Of Abnormal Pregnancy Outcome.

Degree: PhD, Physiology, 2015, Wayne State University

  The placenta is vital for the short- and long-term health of the fetus, and significantly impacts the health of the mother. During the first… (more)

Subjects/Keywords: Early Pregnancy Loss; Extravillous trophoblast cells; Placenta; Preeclampsia; Prenatal Diagnosis; Physiology

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Fritz, R. (2015). Trophoblast Retrieval And Isolation From The Cervix (tric) For Non-Invasive Prenatal Genetic Diagnosis And Prediction Of Abnormal Pregnancy Outcome. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1310

Chicago Manual of Style (16th Edition):

Fritz, Rani. “Trophoblast Retrieval And Isolation From The Cervix (tric) For Non-Invasive Prenatal Genetic Diagnosis And Prediction Of Abnormal Pregnancy Outcome.” 2015. Doctoral Dissertation, Wayne State University. Accessed October 13, 2019. https://digitalcommons.wayne.edu/oa_dissertations/1310.

MLA Handbook (7th Edition):

Fritz, Rani. “Trophoblast Retrieval And Isolation From The Cervix (tric) For Non-Invasive Prenatal Genetic Diagnosis And Prediction Of Abnormal Pregnancy Outcome.” 2015. Web. 13 Oct 2019.

Vancouver:

Fritz R. Trophoblast Retrieval And Isolation From The Cervix (tric) For Non-Invasive Prenatal Genetic Diagnosis And Prediction Of Abnormal Pregnancy Outcome. [Internet] [Doctoral dissertation]. Wayne State University; 2015. [cited 2019 Oct 13]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1310.

Council of Science Editors:

Fritz R. Trophoblast Retrieval And Isolation From The Cervix (tric) For Non-Invasive Prenatal Genetic Diagnosis And Prediction Of Abnormal Pregnancy Outcome. [Doctoral Dissertation]. Wayne State University; 2015. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1310


University of South Carolina

26. Anderson, Sabrina. An Exploration of the Genetic Counselor-Patient Relationship Following a Life-limiting Prenatal Diagnosis.

Degree: MS, Genetic Counseling, 2015, University of South Carolina

  The proposed Reciprocal-Engagement Model of genetic counseling is comprised of five core tenets with the relationship between the genetic counselor and patient being central… (more)

Subjects/Keywords: genetic counseling; genetic counselor-patient relationship; life-limiting prenatal diagnosis

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Anderson, S. (2015). An Exploration of the Genetic Counselor-Patient Relationship Following a Life-limiting Prenatal Diagnosis. (Masters Thesis). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/4536

Chicago Manual of Style (16th Edition):

Anderson, Sabrina. “An Exploration of the Genetic Counselor-Patient Relationship Following a Life-limiting Prenatal Diagnosis.” 2015. Masters Thesis, University of South Carolina. Accessed October 13, 2019. https://scholarcommons.sc.edu/etd/4536.

MLA Handbook (7th Edition):

Anderson, Sabrina. “An Exploration of the Genetic Counselor-Patient Relationship Following a Life-limiting Prenatal Diagnosis.” 2015. Web. 13 Oct 2019.

Vancouver:

Anderson S. An Exploration of the Genetic Counselor-Patient Relationship Following a Life-limiting Prenatal Diagnosis. [Internet] [Masters thesis]. University of South Carolina; 2015. [cited 2019 Oct 13]. Available from: https://scholarcommons.sc.edu/etd/4536.

Council of Science Editors:

Anderson S. An Exploration of the Genetic Counselor-Patient Relationship Following a Life-limiting Prenatal Diagnosis. [Masters Thesis]. University of South Carolina; 2015. Available from: https://scholarcommons.sc.edu/etd/4536


Uppsala University

27. Ortman, Agnes. Increased knowledge and parents fertility decisions. The effect of the CUB-test on abortions.

Degree: Economics, 2019, Uppsala University

  New and more advanced prenatal tests have steadily been introduced in the Swedish maternity care system in the last 30 years. The combined test,… (more)

Subjects/Keywords: Prenatal diagnosis; CUB; chromosomal aberrations; health economics; Economics; Nationalekonomi

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ortman, A. (2019). Increased knowledge and parents fertility decisions. The effect of the CUB-test on abortions. (Thesis). Uppsala University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-388813

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ortman, Agnes. “Increased knowledge and parents fertility decisions. The effect of the CUB-test on abortions.” 2019. Thesis, Uppsala University. Accessed October 13, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-388813.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ortman, Agnes. “Increased knowledge and parents fertility decisions. The effect of the CUB-test on abortions.” 2019. Web. 13 Oct 2019.

Vancouver:

Ortman A. Increased knowledge and parents fertility decisions. The effect of the CUB-test on abortions. [Internet] [Thesis]. Uppsala University; 2019. [cited 2019 Oct 13]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-388813.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ortman A. Increased knowledge and parents fertility decisions. The effect of the CUB-test on abortions. [Thesis]. Uppsala University; 2019. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-388813

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

28. Jahodova, M.G.J. Klinische aspecten van de prenatale diagnostiek.

Degree: 1975, Erasmus University Medical Center

 textabstractPrenatal diagnosis of a number of severe is possible by amniocentesis in the 14th pregnancy and the subsequent analysis of genetic disorders 16th week of… (more)

Subjects/Keywords: early pregnancy; prenatal diagnosis

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Jahodova, M. G. J. (1975). Klinische aspecten van de prenatale diagnostiek. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/31398

Chicago Manual of Style (16th Edition):

Jahodova, M G J. “Klinische aspecten van de prenatale diagnostiek.” 1975. Doctoral Dissertation, Erasmus University Medical Center. Accessed October 13, 2019. http://hdl.handle.net/1765/31398.

MLA Handbook (7th Edition):

Jahodova, M G J. “Klinische aspecten van de prenatale diagnostiek.” 1975. Web. 13 Oct 2019.

Vancouver:

Jahodova MGJ. Klinische aspecten van de prenatale diagnostiek. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 1975. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/1765/31398.

Council of Science Editors:

Jahodova MGJ. Klinische aspecten van de prenatale diagnostiek. [Doctoral Dissertation]. Erasmus University Medical Center; 1975. Available from: http://hdl.handle.net/1765/31398


University of Arizona

29. Hauck, Lynn. A descriptive study of women's reactions to amniocentesis and prenatal genetic studies .

Degree: 1980, University of Arizona

Subjects/Keywords: Amniocentesis.; Genetic counseling.; Prenatal diagnosis.

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Hauck, L. (1980). A descriptive study of women's reactions to amniocentesis and prenatal genetic studies . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/557502

Chicago Manual of Style (16th Edition):

Hauck, Lynn. “A descriptive study of women's reactions to amniocentesis and prenatal genetic studies .” 1980. Masters Thesis, University of Arizona. Accessed October 13, 2019. http://hdl.handle.net/10150/557502.

MLA Handbook (7th Edition):

Hauck, Lynn. “A descriptive study of women's reactions to amniocentesis and prenatal genetic studies .” 1980. Web. 13 Oct 2019.

Vancouver:

Hauck L. A descriptive study of women's reactions to amniocentesis and prenatal genetic studies . [Internet] [Masters thesis]. University of Arizona; 1980. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10150/557502.

Council of Science Editors:

Hauck L. A descriptive study of women's reactions to amniocentesis and prenatal genetic studies . [Masters Thesis]. University of Arizona; 1980. Available from: http://hdl.handle.net/10150/557502


Universitat de Barcelona

30. Rodríguez Pérez, Mª Ángeles. Valoración ecográfica prenatal del cono medular fetal.

Degree: 2016, Universitat de Barcelona

 Subtle skin-covered spinal dysraphism are very difficult to detect in utero due to their lack of intracranial anomalies. They are usually associated to tethered cord… (more)

Subjects/Keywords: Espina bífida; Spina bifida; Diagnòstic prenatal; Diagnóstico prenatal; Prenatal diagnosis; Ecografia fetal; Ecografía fetal; Fetal ultrasonic imaging; Ciències de la Salut; 616.8

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APA (6th Edition):

Rodríguez Pérez, M. . (2016). Valoración ecográfica prenatal del cono medular fetal. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/397729

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rodríguez Pérez, Mª Ángeles. “Valoración ecográfica prenatal del cono medular fetal.” 2016. Thesis, Universitat de Barcelona. Accessed October 13, 2019. http://hdl.handle.net/10803/397729.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rodríguez Pérez, Mª Ángeles. “Valoración ecográfica prenatal del cono medular fetal.” 2016. Web. 13 Oct 2019.

Vancouver:

Rodríguez Pérez M. Valoración ecográfica prenatal del cono medular fetal. [Internet] [Thesis]. Universitat de Barcelona; 2016. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10803/397729.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rodríguez Pérez M. Valoración ecográfica prenatal del cono medular fetal. [Thesis]. Universitat de Barcelona; 2016. Available from: http://hdl.handle.net/10803/397729

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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