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You searched for subject:(X chromosome Abnormalities). Showing records 1 – 15 of 15 total matches.

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University of Gothenburg / Göteborgs Universitet

1. Olanders, Staffan, 1928-. Kvinnor med övertaliga X-kromosomer : en studie av 39 psykiska fall.

Degree: 1974, University of Gothenburg / Göteborgs Universitet

Subjects/Keywords: X chromosome: abnormalities

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APA (6th Edition):

Olanders, Staffan, 1. (1974). Kvinnor med övertaliga X-kromosomer : en studie av 39 psykiska fall. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/13429

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):

Olanders, Staffan, 1928-. “Kvinnor med övertaliga X-kromosomer : en studie av 39 psykiska fall.” 1974. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed December 15, 2019. http://hdl.handle.net/2077/13429.

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

MLA Handbook (7th Edition):

Olanders, Staffan, 1928-. “Kvinnor med övertaliga X-kromosomer : en studie av 39 psykiska fall.” 1974. Web. 15 Dec 2019.

Vancouver:

Olanders, Staffan 1. Kvinnor med övertaliga X-kromosomer : en studie av 39 psykiska fall. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 1974. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2077/13429.

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

Council of Science Editors:

Olanders, Staffan 1. Kvinnor med övertaliga X-kromosomer : en studie av 39 psykiska fall. [Thesis]. University of Gothenburg / Göteborgs Universitet; 1974. Available from: http://hdl.handle.net/2077/13429

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


McGill University

2. Sabbaghian, Nelly. Structure-function analysis of three widely dispersed point mutations in the hormone-binding domain of the human androgen receptor.

Degree: MS, Department of Biology., 1994, McGill University

 Three point mutations have been found in the hormone-binding domain (HBD) of the human androgen receptor (hAR): one in the N-terminal end (Ile663Asn in a… (more)

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

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APA (6th Edition):

Sabbaghian, N. (1994). Structure-function analysis of three widely dispersed point mutations in the hormone-binding domain of the human androgen receptor. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile68254.pdf

Chicago Manual of Style (16th Edition):

Sabbaghian, Nelly. “Structure-function analysis of three widely dispersed point mutations in the hormone-binding domain of the human androgen receptor.” 1994. Masters Thesis, McGill University. Accessed December 15, 2019. http://digitool.library.mcgill.ca/thesisfile68254.pdf.

MLA Handbook (7th Edition):

Sabbaghian, Nelly. “Structure-function analysis of three widely dispersed point mutations in the hormone-binding domain of the human androgen receptor.” 1994. Web. 15 Dec 2019.

Vancouver:

Sabbaghian N. Structure-function analysis of three widely dispersed point mutations in the hormone-binding domain of the human androgen receptor. [Internet] [Masters thesis]. McGill University; 1994. [cited 2019 Dec 15]. Available from: http://digitool.library.mcgill.ca/thesisfile68254.pdf.

Council of Science Editors:

Sabbaghian N. Structure-function analysis of three widely dispersed point mutations in the hormone-binding domain of the human androgen receptor. [Masters Thesis]. McGill University; 1994. Available from: http://digitool.library.mcgill.ca/thesisfile68254.pdf


McGill University

3. 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 December 15, 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. 15 Dec 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 Dec 15]. 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

4. 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 (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 December 15, 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. 15 Dec 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 Dec 15]. 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


McGill University

5. Prior, Lynn. Molecular genetic analysis of receptor-defective androgen resistance in man.

Degree: MS, Department of Biology., 1989, McGill University

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

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APA (6th Edition):

Prior, L. (1989). Molecular genetic analysis of receptor-defective androgen resistance in man. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile55646.pdf

Chicago Manual of Style (16th Edition):

Prior, Lynn. “Molecular genetic analysis of receptor-defective androgen resistance in man.” 1989. Masters Thesis, McGill University. Accessed December 15, 2019. http://digitool.library.mcgill.ca/thesisfile55646.pdf.

MLA Handbook (7th Edition):

Prior, Lynn. “Molecular genetic analysis of receptor-defective androgen resistance in man.” 1989. Web. 15 Dec 2019.

Vancouver:

Prior L. Molecular genetic analysis of receptor-defective androgen resistance in man. [Internet] [Masters thesis]. McGill University; 1989. [cited 2019 Dec 15]. Available from: http://digitool.library.mcgill.ca/thesisfile55646.pdf.

Council of Science Editors:

Prior L. Molecular genetic analysis of receptor-defective androgen resistance in man. [Masters Thesis]. McGill University; 1989. Available from: http://digitool.library.mcgill.ca/thesisfile55646.pdf


McGill University

6. Mhatre, Anand N. Biochemical and molecular genetic analysis of mutant androgen receptors in humans.

Degree: PhD, Department of Biology., 1992, McGill University

The major objective of this thesis was to determine the molecular basis of a "ligand-selective" mutant androgen receptor (AR) phenotype. Methyltrienelone (MT), a synthetic androgen,… (more)

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

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APA (6th Edition):

Mhatre, A. N. (1992). Biochemical and molecular genetic analysis of mutant androgen receptors in humans. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile39499.pdf

Chicago Manual of Style (16th Edition):

Mhatre, Anand N. “Biochemical and molecular genetic analysis of mutant androgen receptors in humans.” 1992. Doctoral Dissertation, McGill University. Accessed December 15, 2019. http://digitool.library.mcgill.ca/thesisfile39499.pdf.

MLA Handbook (7th Edition):

Mhatre, Anand N. “Biochemical and molecular genetic analysis of mutant androgen receptors in humans.” 1992. Web. 15 Dec 2019.

Vancouver:

Mhatre AN. Biochemical and molecular genetic analysis of mutant androgen receptors in humans. [Internet] [Doctoral dissertation]. McGill University; 1992. [cited 2019 Dec 15]. Available from: http://digitool.library.mcgill.ca/thesisfile39499.pdf.

Council of Science Editors:

Mhatre AN. Biochemical and molecular genetic analysis of mutant androgen receptors in humans. [Doctoral Dissertation]. McGill University; 1992. Available from: http://digitool.library.mcgill.ca/thesisfile39499.pdf


McGill University

7. Bordet, Sylvie. Analysis of two point mutations in the androgen receptor gene of patients with complete androgen resistance.

Degree: MS, Department of Biology., 1992, McGill University

 Two previously identified sequence alterations in the androgen receptor gene of patients with complete androgen resistance are studied to prove their pathogenicity. Family studies confirm… (more)

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

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APA (6th Edition):

Bordet, S. (1992). Analysis of two point mutations in the androgen receptor gene of patients with complete androgen resistance. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile56917.pdf

Chicago Manual of Style (16th Edition):

Bordet, Sylvie. “Analysis of two point mutations in the androgen receptor gene of patients with complete androgen resistance.” 1992. Masters Thesis, McGill University. Accessed December 15, 2019. http://digitool.library.mcgill.ca/thesisfile56917.pdf.

MLA Handbook (7th Edition):

Bordet, Sylvie. “Analysis of two point mutations in the androgen receptor gene of patients with complete androgen resistance.” 1992. Web. 15 Dec 2019.

Vancouver:

Bordet S. Analysis of two point mutations in the androgen receptor gene of patients with complete androgen resistance. [Internet] [Masters thesis]. McGill University; 1992. [cited 2019 Dec 15]. Available from: http://digitool.library.mcgill.ca/thesisfile56917.pdf.

Council of Science Editors:

Bordet S. Analysis of two point mutations in the androgen receptor gene of patients with complete androgen resistance. [Masters Thesis]. McGill University; 1992. Available from: http://digitool.library.mcgill.ca/thesisfile56917.pdf

8. Coultas, Susan L. (Susan Lynette). A comparison of straight-stained, Q-stained, and reverse flourescent-stained cell lines for detection of fragile sites on the human X chromosome.

Degree: 1985, North Texas State University

Cell cultures were examined for percentage of fragile sites seen in straight-stained, Q-stained and reverse fluorescent-stained preparations. In all cases, percentage of fragile site expression was decreased when compared to straight-stained preparations. However, fragile sites seen in Q- and RF-stain could be identified as on X chromosomes.

Subjects/Keywords: human chromosome abnormalities; chromosomes; fragile x syndrome

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APA (6th Edition):

Coultas, S. L. (. L. (1985). A comparison of straight-stained, Q-stained, and reverse flourescent-stained cell lines for detection of fragile sites on the human X chromosome. (Thesis). North Texas State University. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc798127/

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):

Coultas, Susan L (Susan Lynette). “A comparison of straight-stained, Q-stained, and reverse flourescent-stained cell lines for detection of fragile sites on the human X chromosome.” 1985. Thesis, North Texas State University. Accessed December 15, 2019. https://digital.library.unt.edu/ark:/67531/metadc798127/.

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

MLA Handbook (7th Edition):

Coultas, Susan L (Susan Lynette). “A comparison of straight-stained, Q-stained, and reverse flourescent-stained cell lines for detection of fragile sites on the human X chromosome.” 1985. Web. 15 Dec 2019.

Vancouver:

Coultas SL(L. A comparison of straight-stained, Q-stained, and reverse flourescent-stained cell lines for detection of fragile sites on the human X chromosome. [Internet] [Thesis]. North Texas State University; 1985. [cited 2019 Dec 15]. Available from: https://digital.library.unt.edu/ark:/67531/metadc798127/.

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

Council of Science Editors:

Coultas SL(L. A comparison of straight-stained, Q-stained, and reverse flourescent-stained cell lines for detection of fragile sites on the human X chromosome. [Thesis]. North Texas State University; 1985. Available from: https://digital.library.unt.edu/ark:/67531/metadc798127/

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


McGill University

9. Popovich, Bradley W. (Bradley Wayne). Folate studies on cultured cells from patients with the fragile X syndrome.

Degree: MS, Department of Biology, 1982, McGill University

Subjects/Keywords: Folic acid  – Metabolism.; Mental retardation  – Genetic aspects.; X chromosome  – Abnormalities.; Fragile X syndrome.

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APA (6th Edition):

Popovich, B. W. (. W. (1982). Folate studies on cultured cells from patients with the fragile X syndrome. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile62480.pdf

Chicago Manual of Style (16th Edition):

Popovich, Bradley W (Bradley Wayne). “Folate studies on cultured cells from patients with the fragile X syndrome.” 1982. Masters Thesis, McGill University. Accessed December 15, 2019. http://digitool.library.mcgill.ca/thesisfile62480.pdf.

MLA Handbook (7th Edition):

Popovich, Bradley W (Bradley Wayne). “Folate studies on cultured cells from patients with the fragile X syndrome.” 1982. Web. 15 Dec 2019.

Vancouver:

Popovich BW(W. Folate studies on cultured cells from patients with the fragile X syndrome. [Internet] [Masters thesis]. McGill University; 1982. [cited 2019 Dec 15]. Available from: http://digitool.library.mcgill.ca/thesisfile62480.pdf.

Council of Science Editors:

Popovich BW(W. Folate studies on cultured cells from patients with the fragile X syndrome. [Masters Thesis]. McGill University; 1982. Available from: http://digitool.library.mcgill.ca/thesisfile62480.pdf


University of Adelaide

10. 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 December 15, 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. 15 Dec 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 Dec 15]. 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


University of Oxford

11. Chen, Zheng-Yi. Molecular biology of X-chromosome disease.

Degree: 1992, University of Oxford

 Genomic clones were isolated and characterized using the human monoamine oxidase A (MAOA) cDNA to screen a phage library, constructed from a human 4X cell… (more)

Subjects/Keywords: 572.8; X chromosome : Molecular aspects : Abnormalities : Genetic disorders : Monoamine oxidase

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APA (6th Edition):

Chen, Z. (1992). Molecular biology of X-chromosome disease. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:8214a2f6-0bfa-4ea4-8f48-b8a20f29318c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317897

Chicago Manual of Style (16th Edition):

Chen, Zheng-Yi. “Molecular biology of X-chromosome disease.” 1992. Doctoral Dissertation, University of Oxford. Accessed December 15, 2019. http://ora.ox.ac.uk/objects/uuid:8214a2f6-0bfa-4ea4-8f48-b8a20f29318c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317897.

MLA Handbook (7th Edition):

Chen, Zheng-Yi. “Molecular biology of X-chromosome disease.” 1992. Web. 15 Dec 2019.

Vancouver:

Chen Z. Molecular biology of X-chromosome disease. [Internet] [Doctoral dissertation]. University of Oxford; 1992. [cited 2019 Dec 15]. Available from: http://ora.ox.ac.uk/objects/uuid:8214a2f6-0bfa-4ea4-8f48-b8a20f29318c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317897.

Council of Science Editors:

Chen Z. Molecular biology of X-chromosome disease. [Doctoral Dissertation]. University of Oxford; 1992. Available from: http://ora.ox.ac.uk/objects/uuid:8214a2f6-0bfa-4ea4-8f48-b8a20f29318c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317897


McGill University

12. 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 December 15, 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. 15 Dec 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 Dec 15]. 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

13. Lyman, Janet K. An X Chromatin Survey at Woodward State Hospital and Training School, an Institution for the Mentally Retarded .

Degree: 1975, Drake U

 The problem. The majority of the Woodward State hospital and training school population was surveyed to locate and identify residents with X chromatin abnormalities. Procedure.… (more)

Subjects/Keywords: Psychiatric hospitals – Surveys; People with mental disabilities – Institutional care – Surveys; X chromosome – Abnormalities – Surveys; X-linked mental retardation – Surveys

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APA (6th Edition):

Lyman, J. K. (1975). An X Chromatin Survey at Woodward State Hospital and Training School, an Institution for the Mentally Retarded . (Thesis). Drake U. Retrieved from http://hdl.handle.net/2092/877

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):

Lyman, Janet K. “An X Chromatin Survey at Woodward State Hospital and Training School, an Institution for the Mentally Retarded .” 1975. Thesis, Drake U. Accessed December 15, 2019. http://hdl.handle.net/2092/877.

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

MLA Handbook (7th Edition):

Lyman, Janet K. “An X Chromatin Survey at Woodward State Hospital and Training School, an Institution for the Mentally Retarded .” 1975. Web. 15 Dec 2019.

Vancouver:

Lyman JK. An X Chromatin Survey at Woodward State Hospital and Training School, an Institution for the Mentally Retarded . [Internet] [Thesis]. Drake U; 1975. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2092/877.

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

Council of Science Editors:

Lyman JK. An X Chromatin Survey at Woodward State Hospital and Training School, an Institution for the Mentally Retarded . [Thesis]. Drake U; 1975. Available from: http://hdl.handle.net/2092/877

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


University of Adelaide

14. Suthers, Graeme Kemble. The human gene map near the fragile X / by Graeme Kemble Suthers.

Degree: 1990, University of Adelaide

Subjects/Keywords: 616.85/88042 20; Fragile X syndrome.; Human chromosome abnormalities.; Linkage (Genetics); Mental retardation Genetic aspects.

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APA (6th Edition):

Suthers, G. K. (1990). The human gene map near the fragile X / by Graeme Kemble Suthers. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/19331

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):

Suthers, Graeme Kemble. “The human gene map near the fragile X / by Graeme Kemble Suthers.” 1990. Thesis, University of Adelaide. Accessed December 15, 2019. http://hdl.handle.net/2440/19331.

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

MLA Handbook (7th Edition):

Suthers, Graeme Kemble. “The human gene map near the fragile X / by Graeme Kemble Suthers.” 1990. Web. 15 Dec 2019.

Vancouver:

Suthers GK. The human gene map near the fragile X / by Graeme Kemble Suthers. [Internet] [Thesis]. University of Adelaide; 1990. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2440/19331.

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

Council of Science Editors:

Suthers GK. The human gene map near the fragile X / by Graeme Kemble Suthers. [Thesis]. University of Adelaide; 1990. Available from: http://hdl.handle.net/2440/19331

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


University of Adelaide

15. Lapsys, N. M. The FRA 16B locus : long range restriction mapping of 16q13 - 16q22.1 / by Naras Mykolas Lapsys.

Degree: 1993, University of Adelaide

Summary: Primary object ... was to construct a pulsed field gel electrophoresis (PFGE) derived long range restriction map of this region by physically linking adjacent DNA probes to common high molecular weight genomic DNA fragments Advisors/Committee Members: Dept. of Paediatrics (school).

Subjects/Keywords: 611/.01816; 574.87322 20; Fragile X syndrome.; Human chromosome abnormalities.; Molecular cloning.; Human gene mapping.; Linkage (Genetics)

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APA (6th Edition):

Lapsys, N. M. (1993). The FRA 16B locus : long range restriction mapping of 16q13 - 16q22.1 / by Naras Mykolas Lapsys. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/21413

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):

Lapsys, N M. “The FRA 16B locus : long range restriction mapping of 16q13 - 16q22.1 / by Naras Mykolas Lapsys.” 1993. Thesis, University of Adelaide. Accessed December 15, 2019. http://hdl.handle.net/2440/21413.

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

MLA Handbook (7th Edition):

Lapsys, N M. “The FRA 16B locus : long range restriction mapping of 16q13 - 16q22.1 / by Naras Mykolas Lapsys.” 1993. Web. 15 Dec 2019.

Vancouver:

Lapsys NM. The FRA 16B locus : long range restriction mapping of 16q13 - 16q22.1 / by Naras Mykolas Lapsys. [Internet] [Thesis]. University of Adelaide; 1993. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2440/21413.

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

Council of Science Editors:

Lapsys NM. The FRA 16B locus : long range restriction mapping of 16q13 - 16q22.1 / by Naras Mykolas Lapsys. [Thesis]. University of Adelaide; 1993. Available from: http://hdl.handle.net/2440/21413

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

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