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Dates: 1995 – 1999

You searched for subject:(Chromosome). Showing records 1 – 30 of 54 total matches.

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Oregon State University

1. Gale, William L. Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone.

Degree: MS, Fisheries Science, 1996, Oregon State University

Subjects/Keywords: Chromosome inversions

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APA (6th Edition):

Gale, W. L. (1996). Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/34815

Chicago Manual of Style (16th Edition):

Gale, William L. “Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone.” 1996. Masters Thesis, Oregon State University. Accessed November 19, 2019. http://hdl.handle.net/1957/34815.

MLA Handbook (7th Edition):

Gale, William L. “Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone.” 1996. Web. 19 Nov 2019.

Vancouver:

Gale WL. Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone. [Internet] [Masters thesis]. Oregon State University; 1996. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/1957/34815.

Council of Science Editors:

Gale WL. Sexual differentiation and steroid-induced sex inversion in Nile tilapia (Oreochromis niloticus) : 1. Characterization of a gonadal androgen receptor : 2. Masculinization by immersion in methyldihydrotestosterone. [Masters Thesis]. Oregon State University; 1996. Available from: http://hdl.handle.net/1957/34815

2. Gault, Judith M. Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias.

Degree: PhD, 1995, Oregon Health Sciences University

Subjects/Keywords: Ectodermal Dysplasia  – genetics; X Chromosome; Cloning, Molecular; Chromosome Mapping

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APA (6th Edition):

Gault, J. M. (1995). Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4F47MC8 ; http://digitalcommons.ohsu.edu/etd/2752

Chicago Manual of Style (16th Edition):

Gault, Judith M. “Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias.” 1995. Doctoral Dissertation, Oregon Health Sciences University. Accessed November 19, 2019. doi:10.6083/M4F47MC8 ; http://digitalcommons.ohsu.edu/etd/2752.

MLA Handbook (7th Edition):

Gault, Judith M. “Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias.” 1995. Web. 19 Nov 2019.

Vancouver:

Gault JM. Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1995. [cited 2019 Nov 19]. Available from: doi:10.6083/M4F47MC8 ; http://digitalcommons.ohsu.edu/etd/2752.

Council of Science Editors:

Gault JM. Molecular genetic studies of two forms of x-linked hypohidrotic ectodermal dysplasias. [Doctoral Dissertation]. Oregon Health Sciences University; 1995. Available from: doi:10.6083/M4F47MC8 ; http://digitalcommons.ohsu.edu/etd/2752


McGill University

3. Demczuk, Suzanne. Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions.

Degree: PhD, Department of Biology., 1995, McGill University

DiGeorge syndrome (DGS) is a developmental defect associated with deletions in chromosomal region 22q11.2. Recently, other syndromes (Velo-Cardio-Facial syndrome, Conotruncal Anomaly Face syndrome, isolated conotruncal… (more)

Subjects/Keywords: Human chromosome abnormalities; Human cytogenetics

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APA (6th Edition):

Demczuk, S. (1995). Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile28726.pdf

Chicago Manual of Style (16th Edition):

Demczuk, Suzanne. “Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions.” 1995. Doctoral Dissertation, McGill University. Accessed November 19, 2019. http://digitool.library.mcgill.ca/thesisfile28726.pdf.

MLA Handbook (7th Edition):

Demczuk, Suzanne. “Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions.” 1995. Web. 19 Nov 2019.

Vancouver:

Demczuk S. Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions. [Internet] [Doctoral dissertation]. McGill University; 1995. [cited 2019 Nov 19]. Available from: http://digitool.library.mcgill.ca/thesisfile28726.pdf.

Council of Science Editors:

Demczuk S. Genetic characterization of DiGeorge and related syndromes associated with 22q11.2 deletions. [Doctoral Dissertation]. McGill University; 1995. Available from: http://digitool.library.mcgill.ca/thesisfile28726.pdf


University of Adelaide

4. Nancarrow, Julie K. Studies of fragile sites on human chromosome 16 / Julie Nancarrow.

Degree: 1998, University of Adelaide

Subjects/Keywords: Human chromosome 16 Abnormalities.

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APA (6th Edition):

Nancarrow, J. K. (1998). Studies of fragile sites on human chromosome 16 / Julie Nancarrow. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/19280

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):

Nancarrow, Julie K. “Studies of fragile sites on human chromosome 16 / Julie Nancarrow.” 1998. Thesis, University of Adelaide. Accessed November 19, 2019. http://hdl.handle.net/2440/19280.

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

MLA Handbook (7th Edition):

Nancarrow, Julie K. “Studies of fragile sites on human chromosome 16 / Julie Nancarrow.” 1998. Web. 19 Nov 2019.

Vancouver:

Nancarrow JK. Studies of fragile sites on human chromosome 16 / Julie Nancarrow. [Internet] [Thesis]. University of Adelaide; 1998. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/2440/19280.

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

Council of Science Editors:

Nancarrow JK. Studies of fragile sites on human chromosome 16 / Julie Nancarrow. [Thesis]. University of Adelaide; 1998. Available from: http://hdl.handle.net/2440/19280

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


University of Adelaide

5. Downie-Doyle, Sarah Elizabeth. Detection of chromosomes and chromosomal abnormalities in human sperm / Sarah Elizabeth Downie.

Degree: 1999, University of Adelaide

 A study of chromosomal abnormalities and the localisation of chromosomes in human sperm, especially from men with TSD, using fluorescence in situ hybridization (FISH). The… (more)

Subjects/Keywords: Spermatozoa Physiology.; Chromosome abnormalities.

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APA (6th Edition):

Downie-Doyle, S. E. (1999). Detection of chromosomes and chromosomal abnormalities in human sperm / Sarah Elizabeth Downie. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/19769

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):

Downie-Doyle, Sarah Elizabeth. “Detection of chromosomes and chromosomal abnormalities in human sperm / Sarah Elizabeth Downie.” 1999. Thesis, University of Adelaide. Accessed November 19, 2019. http://hdl.handle.net/2440/19769.

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

MLA Handbook (7th Edition):

Downie-Doyle, Sarah Elizabeth. “Detection of chromosomes and chromosomal abnormalities in human sperm / Sarah Elizabeth Downie.” 1999. Web. 19 Nov 2019.

Vancouver:

Downie-Doyle SE. Detection of chromosomes and chromosomal abnormalities in human sperm / Sarah Elizabeth Downie. [Internet] [Thesis]. University of Adelaide; 1999. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/2440/19769.

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

Council of Science Editors:

Downie-Doyle SE. Detection of chromosomes and chromosomal abnormalities in human sperm / Sarah Elizabeth Downie. [Thesis]. University of Adelaide; 1999. Available from: http://hdl.handle.net/2440/19769

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


University of Glasgow

6. Ghaffari, Saeed R. Development and application of comparative genomic hybridisation (CGH).

Degree: PhD, 1998, University of Glasgow

 The aims of this study were first, to optimise the comparative genomic hybridisation (CGH) technique and test its reliability as a diagnostic tool in a… (more)

Subjects/Keywords: 610; DNA; Chromosome; Clinical genetics

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APA (6th Edition):

Ghaffari, S. R. (1998). Development and application of comparative genomic hybridisation (CGH). (Doctoral Dissertation). University of Glasgow. Retrieved from http://theses.gla.ac.uk/74793/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390763

Chicago Manual of Style (16th Edition):

Ghaffari, Saeed R. “Development and application of comparative genomic hybridisation (CGH).” 1998. Doctoral Dissertation, University of Glasgow. Accessed November 19, 2019. http://theses.gla.ac.uk/74793/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390763.

MLA Handbook (7th Edition):

Ghaffari, Saeed R. “Development and application of comparative genomic hybridisation (CGH).” 1998. Web. 19 Nov 2019.

Vancouver:

Ghaffari SR. Development and application of comparative genomic hybridisation (CGH). [Internet] [Doctoral dissertation]. University of Glasgow; 1998. [cited 2019 Nov 19]. Available from: http://theses.gla.ac.uk/74793/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390763.

Council of Science Editors:

Ghaffari SR. Development and application of comparative genomic hybridisation (CGH). [Doctoral Dissertation]. University of Glasgow; 1998. Available from: http://theses.gla.ac.uk/74793/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390763

7. O'Donovan, Michael Rickard. Extended-term cultures of human T-lymphocytes : characterisation and toxicological applications.

Degree: PhD, 1995, University of Sussex

Subjects/Keywords: 615.9; Chromosome damage; Genotoxicity

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APA (6th Edition):

O'Donovan, M. R. (1995). Extended-term cultures of human T-lymphocytes : characterisation and toxicological applications. (Doctoral Dissertation). University of Sussex. Retrieved from https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283107

Chicago Manual of Style (16th Edition):

O'Donovan, Michael Rickard. “Extended-term cultures of human T-lymphocytes : characterisation and toxicological applications.” 1995. Doctoral Dissertation, University of Sussex. Accessed November 19, 2019. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283107.

MLA Handbook (7th Edition):

O'Donovan, Michael Rickard. “Extended-term cultures of human T-lymphocytes : characterisation and toxicological applications.” 1995. Web. 19 Nov 2019.

Vancouver:

O'Donovan MR. Extended-term cultures of human T-lymphocytes : characterisation and toxicological applications. [Internet] [Doctoral dissertation]. University of Sussex; 1995. [cited 2019 Nov 19]. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283107.

Council of Science Editors:

O'Donovan MR. Extended-term cultures of human T-lymphocytes : characterisation and toxicological applications. [Doctoral Dissertation]. University of Sussex; 1995. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283107


University of Glasgow

8. Mohaddes Ardebili, Seyed Mojtaba. Optimisation of interphase fluorescence in situ hybridisation for detection of common aneuploidies.

Degree: 1996, University of Glasgow

 The optimisation of a simple, reliable and practical method of interphase FISH which allows prenatal diagnosis of major chromosome aneuploidies using a minimum volume of… (more)

Subjects/Keywords: 572.8; Prenatal diagnosis of chromosome aneupoloidies

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APA (6th Edition):

Mohaddes Ardebili, S. M. (1996). Optimisation of interphase fluorescence in situ hybridisation for detection of common aneuploidies. (Doctoral Dissertation). University of Glasgow. Retrieved from http://theses.gla.ac.uk/692/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296981

Chicago Manual of Style (16th Edition):

Mohaddes Ardebili, Seyed Mojtaba. “Optimisation of interphase fluorescence in situ hybridisation for detection of common aneuploidies.” 1996. Doctoral Dissertation, University of Glasgow. Accessed November 19, 2019. http://theses.gla.ac.uk/692/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296981.

MLA Handbook (7th Edition):

Mohaddes Ardebili, Seyed Mojtaba. “Optimisation of interphase fluorescence in situ hybridisation for detection of common aneuploidies.” 1996. Web. 19 Nov 2019.

Vancouver:

Mohaddes Ardebili SM. Optimisation of interphase fluorescence in situ hybridisation for detection of common aneuploidies. [Internet] [Doctoral dissertation]. University of Glasgow; 1996. [cited 2019 Nov 19]. Available from: http://theses.gla.ac.uk/692/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296981.

Council of Science Editors:

Mohaddes Ardebili SM. Optimisation of interphase fluorescence in situ hybridisation for detection of common aneuploidies. [Doctoral Dissertation]. University of Glasgow; 1996. Available from: http://theses.gla.ac.uk/692/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296981


University of South Australia

9. Baraceros, Maria Fe B. Screening for mutations in myotonic disease.

Degree: MAppSc, 1996, University of South Australia

Subjects/Keywords: Human chromosome abnormalities; Myotonia atrophica.; Myotonia congenita.

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APA (6th Edition):

Baraceros, M. F. B. (1996). Screening for mutations in myotonic disease. (Thesis). University of South Australia. Retrieved from http://arrow.unisa.edu.au:8081/1959.8/84489 ; http://arrow.unisa.edu.au/vital/access/manager/Repository/unisa:43117

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):

Baraceros, Maria Fe B. “Screening for mutations in myotonic disease.” 1996. Thesis, University of South Australia. Accessed November 19, 2019. http://arrow.unisa.edu.au:8081/1959.8/84489 ; http://arrow.unisa.edu.au/vital/access/manager/Repository/unisa:43117.

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

MLA Handbook (7th Edition):

Baraceros, Maria Fe B. “Screening for mutations in myotonic disease.” 1996. Web. 19 Nov 2019.

Vancouver:

Baraceros MFB. Screening for mutations in myotonic disease. [Internet] [Thesis]. University of South Australia; 1996. [cited 2019 Nov 19]. Available from: http://arrow.unisa.edu.au:8081/1959.8/84489 ; http://arrow.unisa.edu.au/vital/access/manager/Repository/unisa:43117.

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

Council of Science Editors:

Baraceros MFB. Screening for mutations in myotonic disease. [Thesis]. University of South Australia; 1996. Available from: http://arrow.unisa.edu.au:8081/1959.8/84489 ; http://arrow.unisa.edu.au/vital/access/manager/Repository/unisa:43117

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

10. Madhu, K. Genotoxicity Studies on Liza Parsia and Mugil Cephalus.

Degree: 1995, Cochin University of Science and Technology

Subjects/Keywords: Genotoxicity; Liza Parsia; Mugil Cephalus; Chromosome; Mullets

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APA (6th Edition):

Madhu, K. (1995). Genotoxicity Studies on Liza Parsia and Mugil Cephalus. (Thesis). Cochin University of Science and Technology. Retrieved from http://dyuthi.cusat.ac.in/purl/1895

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):

Madhu, K. “Genotoxicity Studies on Liza Parsia and Mugil Cephalus.” 1995. Thesis, Cochin University of Science and Technology. Accessed November 19, 2019. http://dyuthi.cusat.ac.in/purl/1895.

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

MLA Handbook (7th Edition):

Madhu, K. “Genotoxicity Studies on Liza Parsia and Mugil Cephalus.” 1995. Web. 19 Nov 2019.

Vancouver:

Madhu K. Genotoxicity Studies on Liza Parsia and Mugil Cephalus. [Internet] [Thesis]. Cochin University of Science and Technology; 1995. [cited 2019 Nov 19]. Available from: http://dyuthi.cusat.ac.in/purl/1895.

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

Council of Science Editors:

Madhu K. Genotoxicity Studies on Liza Parsia and Mugil Cephalus. [Thesis]. Cochin University of Science and Technology; 1995. Available from: http://dyuthi.cusat.ac.in/purl/1895

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


University of Alberta

11. Mears, Alan J. Molecular characterization of duplications associated with cat eye syndrome.

Degree: PhD, Department of Genetics, 1995, University of Alberta

Subjects/Keywords: Human chromosome abnormalities.; Genetic disorders.; Gene mapping.

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APA (6th Edition):

Mears, A. J. (1995). Molecular characterization of duplications associated with cat eye syndrome. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/c534fq60m

Chicago Manual of Style (16th Edition):

Mears, Alan J. “Molecular characterization of duplications associated with cat eye syndrome.” 1995. Doctoral Dissertation, University of Alberta. Accessed November 19, 2019. https://era.library.ualberta.ca/files/c534fq60m.

MLA Handbook (7th Edition):

Mears, Alan J. “Molecular characterization of duplications associated with cat eye syndrome.” 1995. Web. 19 Nov 2019.

Vancouver:

Mears AJ. Molecular characterization of duplications associated with cat eye syndrome. [Internet] [Doctoral dissertation]. University of Alberta; 1995. [cited 2019 Nov 19]. Available from: https://era.library.ualberta.ca/files/c534fq60m.

Council of Science Editors:

Mears AJ. Molecular characterization of duplications associated with cat eye syndrome. [Doctoral Dissertation]. University of Alberta; 1995. Available from: https://era.library.ualberta.ca/files/c534fq60m


University of Oulu

12. Grön, M. (Mathias). Effects of human X and Y chromosomes on oral and craniofacial morphology:studies of 46,XY females, 47,XYY males and 45,X/46,XX females.

Degree: 1999, University of Oulu

 Abstract The influence of the X and Y chromosomes on the size and shape of the dental arches and occlusion as well as on craniofacial… (more)

Subjects/Keywords: X inactivation; chromosome aneuploidy; craniofacial complex; dental arches

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APA (6th Edition):

Grön, M. (. (1999). Effects of human X and Y chromosomes on oral and craniofacial morphology:studies of 46,XY females, 47,XYY males and 45,X/46,XX females. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9514253744

Chicago Manual of Style (16th Edition):

Grön, M (Mathias). “Effects of human X and Y chromosomes on oral and craniofacial morphology:studies of 46,XY females, 47,XYY males and 45,X/46,XX females.” 1999. Doctoral Dissertation, University of Oulu. Accessed November 19, 2019. http://urn.fi/urn:isbn:9514253744.

MLA Handbook (7th Edition):

Grön, M (Mathias). “Effects of human X and Y chromosomes on oral and craniofacial morphology:studies of 46,XY females, 47,XYY males and 45,X/46,XX females.” 1999. Web. 19 Nov 2019.

Vancouver:

Grön M(. Effects of human X and Y chromosomes on oral and craniofacial morphology:studies of 46,XY females, 47,XYY males and 45,X/46,XX females. [Internet] [Doctoral dissertation]. University of Oulu; 1999. [cited 2019 Nov 19]. Available from: http://urn.fi/urn:isbn:9514253744.

Council of Science Editors:

Grön M(. Effects of human X and Y chromosomes on oral and craniofacial morphology:studies of 46,XY females, 47,XYY males and 45,X/46,XX females. [Doctoral Dissertation]. University of Oulu; 1999. Available from: http://urn.fi/urn:isbn:9514253744


University of Oulu

13. Launonen, V. (Virpi). Genetic aberrations and their clinical significance in breast and ovarian cancer.

Degree: 1999, University of Oulu

 Abstract In tumourigenesis, genetic alterations accumulate in the genes responsible for cell growth, proliferation and DNA repair: proto-oncogenes, tumour suppressor and DNA repair genes. Inactivation… (more)

Subjects/Keywords: cancer prognosis; chromosome 11; loss of heterozygosity

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APA (6th Edition):

Launonen, V. (. (1999). Genetic aberrations and their clinical significance in breast and ovarian cancer. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9514251946

Chicago Manual of Style (16th Edition):

Launonen, V (Virpi). “Genetic aberrations and their clinical significance in breast and ovarian cancer.” 1999. Doctoral Dissertation, University of Oulu. Accessed November 19, 2019. http://urn.fi/urn:isbn:9514251946.

MLA Handbook (7th Edition):

Launonen, V (Virpi). “Genetic aberrations and their clinical significance in breast and ovarian cancer.” 1999. Web. 19 Nov 2019.

Vancouver:

Launonen V(. Genetic aberrations and their clinical significance in breast and ovarian cancer. [Internet] [Doctoral dissertation]. University of Oulu; 1999. [cited 2019 Nov 19]. Available from: http://urn.fi/urn:isbn:9514251946.

Council of Science Editors:

Launonen V(. Genetic aberrations and their clinical significance in breast and ovarian cancer. [Doctoral Dissertation]. University of Oulu; 1999. Available from: http://urn.fi/urn:isbn:9514251946


University of Oxford

14. Simpson T. Ian, T. Ian. An investigation into the role of methylation in mammalian X-chromosome inactivation.

Degree: 1999, University of Oxford

 X-chromosome inactivation achieves dosage compensation of X-linked genes between male (XY) and female (XX) mammals. This process involves the down-regulation of most, but not all… (more)

Subjects/Keywords: 572.8; Gene silencing : X chromosome : Molecular aspects

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APA (6th Edition):

Simpson T. Ian, T. I. (1999). An investigation into the role of methylation in mammalian X-chromosome inactivation. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:5fd37c27-af19-4bbd-92a7-4c5b846b3a31 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312618

Chicago Manual of Style (16th Edition):

Simpson T. Ian, T Ian. “An investigation into the role of methylation in mammalian X-chromosome inactivation.” 1999. Doctoral Dissertation, University of Oxford. Accessed November 19, 2019. http://ora.ox.ac.uk/objects/uuid:5fd37c27-af19-4bbd-92a7-4c5b846b3a31 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312618.

MLA Handbook (7th Edition):

Simpson T. Ian, T Ian. “An investigation into the role of methylation in mammalian X-chromosome inactivation.” 1999. Web. 19 Nov 2019.

Vancouver:

Simpson T. Ian TI. An investigation into the role of methylation in mammalian X-chromosome inactivation. [Internet] [Doctoral dissertation]. University of Oxford; 1999. [cited 2019 Nov 19]. Available from: http://ora.ox.ac.uk/objects/uuid:5fd37c27-af19-4bbd-92a7-4c5b846b3a31 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312618.

Council of Science Editors:

Simpson T. Ian TI. An investigation into the role of methylation in mammalian X-chromosome inactivation. [Doctoral Dissertation]. University of Oxford; 1999. Available from: http://ora.ox.ac.uk/objects/uuid:5fd37c27-af19-4bbd-92a7-4c5b846b3a31 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312618


University of Oxford

15. Williams, Gareth Owen. Mapping studies of the centromeric region of the human Y chromosome.

Degree: 1998, University of Oxford

 Mapping studies of the centromeric region of the human Y chromosome Construction of a map of a human centromeric region is very important in order… (more)

Subjects/Keywords: 572.8; Human beings : Genome mapping : Y chromosome : Centromere : Analysis

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APA (6th Edition):

Williams, G. O. (1998). Mapping studies of the centromeric region of the human Y chromosome. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:c471a22f-e52b-452a-8714-bfcd9610da44 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244623

Chicago Manual of Style (16th Edition):

Williams, Gareth Owen. “Mapping studies of the centromeric region of the human Y chromosome.” 1998. Doctoral Dissertation, University of Oxford. Accessed November 19, 2019. http://ora.ox.ac.uk/objects/uuid:c471a22f-e52b-452a-8714-bfcd9610da44 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244623.

MLA Handbook (7th Edition):

Williams, Gareth Owen. “Mapping studies of the centromeric region of the human Y chromosome.” 1998. Web. 19 Nov 2019.

Vancouver:

Williams GO. Mapping studies of the centromeric region of the human Y chromosome. [Internet] [Doctoral dissertation]. University of Oxford; 1998. [cited 2019 Nov 19]. Available from: http://ora.ox.ac.uk/objects/uuid:c471a22f-e52b-452a-8714-bfcd9610da44 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244623.

Council of Science Editors:

Williams GO. Mapping studies of the centromeric region of the human Y chromosome. [Doctoral Dissertation]. University of Oxford; 1998. Available from: http://ora.ox.ac.uk/objects/uuid:c471a22f-e52b-452a-8714-bfcd9610da44 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244623


McGill University

16. Fernandes, Maria J. G. Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus.

Degree: PhD, Department of Biology, 1995, McGill University

Note:

Tay-Sachs disease (TSD) is a recessively inherited disorder characterized by the pathological accumulation of GM 2 ganglioside in neuronal cells. Mutations in the HEXA… (more)

Subjects/Keywords: Tay-Sachs disease.; Human chromosome abnormalities  – Diagnosis.

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APA (6th Edition):

Fernandes, M. J. G. (1995). Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile156990.pdf

Chicago Manual of Style (16th Edition):

Fernandes, Maria J G. “Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus.” 1995. Doctoral Dissertation, McGill University. Accessed November 19, 2019. http://digitool.library.mcgill.ca/thesisfile156990.pdf.

MLA Handbook (7th Edition):

Fernandes, Maria J G. “Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus.” 1995. Web. 19 Nov 2019.

Vancouver:

Fernandes MJG. Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus. [Internet] [Doctoral dissertation]. McGill University; 1995. [cited 2019 Nov 19]. Available from: http://digitool.library.mcgill.ca/thesisfile156990.pdf.

Council of Science Editors:

Fernandes MJG. Heteroallelism, Screening and Structure-Function Studies at the Hexa Locus. [Doctoral Dissertation]. McGill University; 1995. Available from: http://digitool.library.mcgill.ca/thesisfile156990.pdf


McGill University

17. Kazemi-Esfarjani, Parsa. Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations.

Degree: PhD, Department of Biology., 1996, McGill University

The human androgen receptor (hAR) is a ligand-activated transcription factor, and like other nuclear receptors, consists of a N-terminal modulatory domain, a central DNA-binding domain,… (more)

Subjects/Keywords: Androgens  – Receptors.; Sex differentiation disorders.; X chromosome  – Abnormalities.

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APA (6th Edition):

Kazemi-Esfarjani, P. (1996). Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile42065.pdf

Chicago Manual of Style (16th Edition):

Kazemi-Esfarjani, Parsa. “Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations.” 1996. Doctoral Dissertation, McGill University. Accessed November 19, 2019. http://digitool.library.mcgill.ca/thesisfile42065.pdf.

MLA Handbook (7th Edition):

Kazemi-Esfarjani, Parsa. “Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations.” 1996. Web. 19 Nov 2019.

Vancouver:

Kazemi-Esfarjani P. Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations. [Internet] [Doctoral dissertation]. McGill University; 1996. [cited 2019 Nov 19]. Available from: http://digitool.library.mcgill.ca/thesisfile42065.pdf.

Council of Science Editors:

Kazemi-Esfarjani P. Functional analysis of the human androgen receptor using synthetic and naturally occurring mutations. [Doctoral Dissertation]. McGill University; 1996. Available from: http://digitool.library.mcgill.ca/thesisfile42065.pdf


McGill University

18. Shkolny, Dana. Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome.

Degree: MS, Department of Biology., 1995, McGill University

 This work proves the pathogenicity of four substitution mutations in the androgen-binding domain of the human androgen receptor (hAR) gene of four subjects with varying… (more)

Subjects/Keywords: Androgens  – Receptors; Sex differentiation disorders; X chromosome  – Abnormalities

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

APA (6th Edition):

Shkolny, D. (1995). Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile23299.pdf

Chicago Manual of Style (16th Edition):

Shkolny, Dana. “Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome.” 1995. Masters Thesis, McGill University. Accessed November 19, 2019. http://digitool.library.mcgill.ca/thesisfile23299.pdf.

MLA Handbook (7th Edition):

Shkolny, Dana. “Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome.” 1995. Web. 19 Nov 2019.

Vancouver:

Shkolny D. Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome. [Internet] [Masters thesis]. McGill University; 1995. [cited 2019 Nov 19]. Available from: http://digitool.library.mcgill.ca/thesisfile23299.pdf.

Council of Science Editors:

Shkolny D. Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome. [Masters Thesis]. McGill University; 1995. Available from: http://digitool.library.mcgill.ca/thesisfile23299.pdf


Michigan State University

19. Liang, Yong. Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness].

Degree: PhD, Graduate Program in Genetics, 1999, Michigan State University

Subjects/Keywords: Deafness – Genetic aspects; Gene mapping; Human chromosome abnormalities

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APA (6th Edition):

Liang, Y. (1999). Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness]. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:27758

Chicago Manual of Style (16th Edition):

Liang, Yong. “Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness].” 1999. Doctoral Dissertation, Michigan State University. Accessed November 19, 2019. http://etd.lib.msu.edu/islandora/object/etd:27758.

MLA Handbook (7th Edition):

Liang, Yong. “Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness].” 1999. Web. 19 Nov 2019.

Vancouver:

Liang Y. Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness]. [Internet] [Doctoral dissertation]. Michigan State University; 1999. [cited 2019 Nov 19]. Available from: http://etd.lib.msu.edu/islandora/object/etd:27758.

Council of Science Editors:

Liang Y. Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness]. [Doctoral Dissertation]. Michigan State University; 1999. Available from: http://etd.lib.msu.edu/islandora/object/etd:27758


University of Gothenburg / Göteborgs Universitet

20. Röijer, Eva 1967-. Physical mapping and cloning of the t(3;8)(p21;q12)translocation breakpoints in pleomorphic adenomas.

Degree: 1997, University of Gothenburg / Göteborgs Universitet

 The pleomorphic adenoma is a benign epithelial tumor originating from the major and minor salivary glands. It is the most common type of salivary gland… (more)

Subjects/Keywords: Pleomorphic adenoma; chromosome abnormalities; positional cloning; fluorescence in situ hybridization (FISH); yeast artificial chromosome (YAC); PLAG1; CTNNB1.

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APA (6th Edition):

Röijer, E. 1. (1997). Physical mapping and cloning of the t(3;8)(p21;q12)translocation breakpoints in pleomorphic adenomas. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/13934

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):

Röijer, Eva 1967-. “Physical mapping and cloning of the t(3;8)(p21;q12)translocation breakpoints in pleomorphic adenomas.” 1997. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed November 19, 2019. http://hdl.handle.net/2077/13934.

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

MLA Handbook (7th Edition):

Röijer, Eva 1967-. “Physical mapping and cloning of the t(3;8)(p21;q12)translocation breakpoints in pleomorphic adenomas.” 1997. Web. 19 Nov 2019.

Vancouver:

Röijer E1. Physical mapping and cloning of the t(3;8)(p21;q12)translocation breakpoints in pleomorphic adenomas. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 1997. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/2077/13934.

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

Council of Science Editors:

Röijer E1. Physical mapping and cloning of the t(3;8)(p21;q12)translocation breakpoints in pleomorphic adenomas. [Thesis]. University of Gothenburg / Göteborgs Universitet; 1997. Available from: http://hdl.handle.net/2077/13934

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

21. Metten, Pamela. Genetics of acute ethanol and benzodiazepine withdrawal severity.

Degree: PhD, 1996, Oregon Health Sciences University

Subjects/Keywords: Substance Withdrawal Syndrome  – genetics; Ethanol; Benzodiazepines; Chromosome Mapping; Mice, Inbred Strains

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APA (6th Edition):

Metten, P. (1996). Genetics of acute ethanol and benzodiazepine withdrawal severity. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4348HMF ; http://digitalcommons.ohsu.edu/etd/2685

Chicago Manual of Style (16th Edition):

Metten, Pamela. “Genetics of acute ethanol and benzodiazepine withdrawal severity.” 1996. Doctoral Dissertation, Oregon Health Sciences University. Accessed November 19, 2019. doi:10.6083/M4348HMF ; http://digitalcommons.ohsu.edu/etd/2685.

MLA Handbook (7th Edition):

Metten, Pamela. “Genetics of acute ethanol and benzodiazepine withdrawal severity.” 1996. Web. 19 Nov 2019.

Vancouver:

Metten P. Genetics of acute ethanol and benzodiazepine withdrawal severity. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1996. [cited 2019 Nov 19]. Available from: doi:10.6083/M4348HMF ; http://digitalcommons.ohsu.edu/etd/2685.

Council of Science Editors:

Metten P. Genetics of acute ethanol and benzodiazepine withdrawal severity. [Doctoral Dissertation]. Oregon Health Sciences University; 1996. Available from: doi:10.6083/M4348HMF ; http://digitalcommons.ohsu.edu/etd/2685

22. Hain, Heather S. Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay.

Degree: PhD, 1999, Oregon Health Sciences University

Subjects/Keywords: Nociceptors  – drug effects; Chromosome Mapping; Morphine; Narcotic Antagonists; Analgesia; Mice, Inbred Strains

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APA (6th Edition):

Hain, H. S. (1999). Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4HX1B09 ; http://digitalcommons.ohsu.edu/etd/3356

Chicago Manual of Style (16th Edition):

Hain, Heather S. “Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay.” 1999. Doctoral Dissertation, Oregon Health Sciences University. Accessed November 19, 2019. doi:10.6083/M4HX1B09 ; http://digitalcommons.ohsu.edu/etd/3356.

MLA Handbook (7th Edition):

Hain, Heather S. “Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay.” 1999. Web. 19 Nov 2019.

Vancouver:

Hain HS. Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1999. [cited 2019 Nov 19]. Available from: doi:10.6083/M4HX1B09 ; http://digitalcommons.ohsu.edu/etd/3356.

Council of Science Editors:

Hain HS. Quantitative trait loci mapping analysis for baseline nociceptive sensitivity and morphine-induced antinociception on the writhing assay. [Doctoral Dissertation]. Oregon Health Sciences University; 1999. Available from: doi:10.6083/M4HX1B09 ; http://digitalcommons.ohsu.edu/etd/3356

23. Rupp, Paul A. Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome.

Degree: PhD, 1999, Oregon Health Sciences University

Subjects/Keywords: Base Sequence; Blotting, Western; Heart Defects, Congenital; Chromosome Deletion; Membrane Proteins  – genetics

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APA (6th Edition):

Rupp, P. A. (1999). Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341

Chicago Manual of Style (16th Edition):

Rupp, Paul A. “Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome.” 1999. Doctoral Dissertation, Oregon Health Sciences University. Accessed November 19, 2019. doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341.

MLA Handbook (7th Edition):

Rupp, Paul A. “Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome.” 1999. Web. 19 Nov 2019.

Vancouver:

Rupp PA. Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1999. [cited 2019 Nov 19]. Available from: doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341.

Council of Science Editors:

Rupp PA. Characterization of cirrin, a candidate for congenital heart defects in 3p- syndrome. [Doctoral Dissertation]. Oregon Health Sciences University; 1999. Available from: doi:10.6083/M4G15Z57 ; http://digitalcommons.ohsu.edu/etd/3341


Massey University

24. Harding, Katherine Mary. Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25.

Degree: MS, Genetics, 1996, Massey University

 The chromosomes of human peripheral blood lymphocytes were analysed for sister chromatid exchanges (SCEs) and structural aberrations and correlated to cigarette smoking habits of 15… (more)

Subjects/Keywords: Human chromosome abnormalities; Smoking  – Health aspects; Women  – Tobacco use; Vanillin  – Health aspects

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APA (6th Edition):

Harding, K. M. (1996). Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/10280

Chicago Manual of Style (16th Edition):

Harding, Katherine Mary. “Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25.” 1996. Masters Thesis, Massey University. Accessed November 19, 2019. http://hdl.handle.net/10179/10280.

MLA Handbook (7th Edition):

Harding, Katherine Mary. “Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25.” 1996. Web. 19 Nov 2019.

Vancouver:

Harding KM. Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25. [Internet] [Masters thesis]. Massey University; 1996. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/10179/10280.

Council of Science Editors:

Harding KM. Effects of cigarette smoking and vanillin concentration on Sister Chromatid Exchange and chromosome aberrations in women aged 16-25. [Masters Thesis]. Massey University; 1996. Available from: http://hdl.handle.net/10179/10280


McGill University

25. Vasiliou, Denise Marie. Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome.

Degree: MS, Department of Biology., 1996, McGill University

 The human androgen receptor (hAR) is a ligand-activated, nuclear transcription factor. Mutations affecting the formation and/or action of the hAR cause androgen insensitivity syndrome (AIS).… (more)

Subjects/Keywords: Androgens  – Receptors.; Exons (Genetics); Sex differentiation disorders.; X chromosome  – Abnormalities.

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APA (6th Edition):

Vasiliou, D. M. (1996). Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile27431.pdf

Chicago Manual of Style (16th Edition):

Vasiliou, Denise Marie. “Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome.” 1996. Masters Thesis, McGill University. Accessed November 19, 2019. http://digitool.library.mcgill.ca/thesisfile27431.pdf.

MLA Handbook (7th Edition):

Vasiliou, Denise Marie. “Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome.” 1996. Web. 19 Nov 2019.

Vancouver:

Vasiliou DM. Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome. [Internet] [Masters thesis]. McGill University; 1996. [cited 2019 Nov 19]. Available from: http://digitool.library.mcgill.ca/thesisfile27431.pdf.

Council of Science Editors:

Vasiliou DM. Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome. [Masters Thesis]. McGill University; 1996. Available from: http://digitool.library.mcgill.ca/thesisfile27431.pdf


University of Oklahoma

26. Crabtree, Judy Sue. Sequencing analysis of regions of human chromosomes 11 and 22: Meningioma (22), cat eye syndrome (22), and multiple endocrine neoplasia, type 1 (11).

Degree: PhD, Department of Chemistry and Biochemistry, 1997, University of Oklahoma

 Analysis to date reveals several putative genes in the MEN-1 region, including the PYGM locus, a zinc finger motif gene, a GC kinase gene, the… (more)

Subjects/Keywords: Meningioma.; Human chromosome abnormalities.; Chemistry, Biochemistry.; Nucleotide sequence.; Biology, Molecular.; Biology, Genetics.

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APA (6th Edition):

Crabtree, J. S. (1997). Sequencing analysis of regions of human chromosomes 11 and 22: Meningioma (22), cat eye syndrome (22), and multiple endocrine neoplasia, type 1 (11). (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/5442

Chicago Manual of Style (16th Edition):

Crabtree, Judy Sue. “Sequencing analysis of regions of human chromosomes 11 and 22: Meningioma (22), cat eye syndrome (22), and multiple endocrine neoplasia, type 1 (11).” 1997. Doctoral Dissertation, University of Oklahoma. Accessed November 19, 2019. http://hdl.handle.net/11244/5442.

MLA Handbook (7th Edition):

Crabtree, Judy Sue. “Sequencing analysis of regions of human chromosomes 11 and 22: Meningioma (22), cat eye syndrome (22), and multiple endocrine neoplasia, type 1 (11).” 1997. Web. 19 Nov 2019.

Vancouver:

Crabtree JS. Sequencing analysis of regions of human chromosomes 11 and 22: Meningioma (22), cat eye syndrome (22), and multiple endocrine neoplasia, type 1 (11). [Internet] [Doctoral dissertation]. University of Oklahoma; 1997. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/11244/5442.

Council of Science Editors:

Crabtree JS. Sequencing analysis of regions of human chromosomes 11 and 22: Meningioma (22), cat eye syndrome (22), and multiple endocrine neoplasia, type 1 (11). [Doctoral Dissertation]. University of Oklahoma; 1997. Available from: http://hdl.handle.net/11244/5442


University of Oklahoma

27. Chen, Feng. Sequence and analysis of approximately 0.5 mega-basepair of the DiGeorge Syndrome Critical Region in human chromosome 22 band q11 and a syntenic mouse BAC.

Degree: PhD, Department of Chemistry and Biochemistry, 1997, University of Oklahoma

 The complete nucleotide sequence of four regions of DiGeorge Sydrome Critical Region in human chromosome 22 band q11, totally 482 kb, and a syntenic mouse… (more)

Subjects/Keywords: Chemistry, Biochemistry.; Biology, Molecular.; Human chromosome abnormalities.; Nucleotide sequence.; Biology, Genetics.

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APA (6th Edition):

Chen, F. (1997). Sequence and analysis of approximately 0.5 mega-basepair of the DiGeorge Syndrome Critical Region in human chromosome 22 band q11 and a syntenic mouse BAC. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/5542

Chicago Manual of Style (16th Edition):

Chen, Feng. “Sequence and analysis of approximately 0.5 mega-basepair of the DiGeorge Syndrome Critical Region in human chromosome 22 band q11 and a syntenic mouse BAC.” 1997. Doctoral Dissertation, University of Oklahoma. Accessed November 19, 2019. http://hdl.handle.net/11244/5542.

MLA Handbook (7th Edition):

Chen, Feng. “Sequence and analysis of approximately 0.5 mega-basepair of the DiGeorge Syndrome Critical Region in human chromosome 22 band q11 and a syntenic mouse BAC.” 1997. Web. 19 Nov 2019.

Vancouver:

Chen F. Sequence and analysis of approximately 0.5 mega-basepair of the DiGeorge Syndrome Critical Region in human chromosome 22 band q11 and a syntenic mouse BAC. [Internet] [Doctoral dissertation]. University of Oklahoma; 1997. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/11244/5542.

Council of Science Editors:

Chen F. Sequence and analysis of approximately 0.5 mega-basepair of the DiGeorge Syndrome Critical Region in human chromosome 22 band q11 and a syntenic mouse BAC. [Doctoral Dissertation]. University of Oklahoma; 1997. Available from: http://hdl.handle.net/11244/5542


University of Adelaide

28. Donnelly, Andrew James. The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly.

Degree: 1997, University of Adelaide

 The aim of the project presented in this thesis is to isolate microsatellite markers and to construct a high resolution genetic map of the human… (more)

Subjects/Keywords: Human gene mapping.; Genetics Research.; Fragile X syndrome.; X chromosome Abnormalities.; Mental retardation.

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APA (6th Edition):

Donnelly, A. J. (1997). The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/19022

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):

Donnelly, Andrew James. “The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly.” 1997. Thesis, University of Adelaide. Accessed November 19, 2019. http://hdl.handle.net/2440/19022.

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

MLA Handbook (7th Edition):

Donnelly, Andrew James. “The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly.” 1997. Web. 19 Nov 2019.

Vancouver:

Donnelly AJ. The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly. [Internet] [Thesis]. University of Adelaide; 1997. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/2440/19022.

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

Council of Science Editors:

Donnelly AJ. The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly. [Thesis]. University of Adelaide; 1997. Available from: http://hdl.handle.net/2440/19022

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

29. Van Dyk, Qinuo Fan. Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men.

Degree: PhD, 1997, Old Dominion University

  The human hemizona has been demonstrated to select spermatozoa with good motility, normal morphology, and the capacity to undergo the zona-induced acrosomal reaction. The… (more)

Subjects/Keywords: Sex chromosome ratios; Aneuploidy rates; Zona pellucida; Spermatozoa; Genetics; Molecular Biology

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APA (6th Edition):

Van Dyk, Q. F. (1997). Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men. (Doctoral Dissertation). Old Dominion University. Retrieved from 9780591631845 ; https://digitalcommons.odu.edu/biomedicalsciences_etds/86

Chicago Manual of Style (16th Edition):

Van Dyk, Qinuo Fan. “Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men.” 1997. Doctoral Dissertation, Old Dominion University. Accessed November 19, 2019. 9780591631845 ; https://digitalcommons.odu.edu/biomedicalsciences_etds/86.

MLA Handbook (7th Edition):

Van Dyk, Qinuo Fan. “Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men.” 1997. Web. 19 Nov 2019.

Vancouver:

Van Dyk QF. Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men. [Internet] [Doctoral dissertation]. Old Dominion University; 1997. [cited 2019 Nov 19]. Available from: 9780591631845 ; https://digitalcommons.odu.edu/biomedicalsciences_etds/86.

Council of Science Editors:

Van Dyk QF. Sex Chromosome Ratios and Aneuploidy Rates in the Zona Pellucida Selected Spermatozoa From Normal and Subfertile Men. [Doctoral Dissertation]. Old Dominion University; 1997. Available from: 9780591631845 ; https://digitalcommons.odu.edu/biomedicalsciences_etds/86


Michigan State University

30. Zubair, Qaisra. An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16.

Degree: MS, Medical Technology Program and Department of Pediatrics and Human Development, 1996, Michigan State University

Subjects/Keywords: Human chromosome abnormalities; Chromosomes – Analysis; Premature infants; Fetal growth retardation – Genetic aspects

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

APA (6th Edition):

Zubair, Q. (1996). An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:26756

Chicago Manual of Style (16th Edition):

Zubair, Qaisra. “An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16.” 1996. Masters Thesis, Michigan State University. Accessed November 19, 2019. http://etd.lib.msu.edu/islandora/object/etd:26756.

MLA Handbook (7th Edition):

Zubair, Qaisra. “An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16.” 1996. Web. 19 Nov 2019.

Vancouver:

Zubair Q. An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16. [Internet] [Masters thesis]. Michigan State University; 1996. [cited 2019 Nov 19]. Available from: http://etd.lib.msu.edu/islandora/object/etd:26756.

Council of Science Editors:

Zubair Q. An investigation of neonatal intensive care unit infants for uniparental disomy : chromosome 16. [Masters Thesis]. Michigan State University; 1996. Available from: http://etd.lib.msu.edu/islandora/object/etd:26756

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