Global ETD Search

11	Analysis of two point mutations in the androgen receptor gene of patients with complete androgen resistance Bordet, Sylvie January 1992 (has links) No description available. Androgens -- Receptors. X chromosome -- Abnormalities. Sex differentiation disorders.
12	Structure-function analysis of three widely dispersed point mutations in the hormone-binding domain of the human androgen receptor Sabbaghian, Nelly January 1994 (has links) No description available. Sex differentiation disorders. Androgens -- Receptors. X chromosome -- Abnormalities.
13	Molecular genetic analysis of receptor-defective androgen resistance in man Prior, Lynn January 1989 (has links) No description available. X chromosome -- Abnormalities. Sex differentiation disorders. Androgens -- Receptors.
14	Analysis of exon 1 and the 5'-flanking region of the androgen receptor gene in subjects with androgen insensitivity syndrome Vasiliou, Denise Marie. January 1996 (has links) No description available. Androgens -- Receptors. Exons (Genetics) X chromosome -- Abnormalities. Sex differentiation disorders.
15	Characterization of four point mutations in the androgen receptor gene of subjects with varying degrees of androgen insensitivity syndrome Shkolny, Dana January 1995 (has links) No description available. Sex differentiation disorders Androgens -- Receptors X chromosome -- Abnormalities
16	Folate studies on cultured cells from patients with the fragile X syndrome Popovich, Bradley W. (Bradley Wayne) January 1982 (has links) No description available. Folic acid -- Metabolism. Mental retardation -- Genetic aspects. X chromosome -- Abnormalities. Fragile X syndrome.
17	The characterisation of human X-linked polymorphic markers and their use in disease gene localisation and identification / Andrew James Donnelly. Donnelly, Andrew James January 1997 (has links) Copies of author's previously published works inserted. / Bibliography: leaves 321-370. / xv, 370, [21] leaves : ill. (chiefly col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / 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 X chromosome using these and pre-existing microsatellite markers. AC dinucleotide repeat markers are isolated from a bacteriophage library for application to the genetic localisations of X-linked disease genes, particularly those responsible for non-specific mental retardation (MRX). The genetic map is used to refine the location of the disease gene segregating in five families affected with X-linked mental retardation. / Thesis (Ph.D.)--University of Adelaide, Dept. of Genetics, 1997 Human gene mapping. Genetics Research. Fragile X syndrome. X chromosome Abnormalities. Mental retardation.
18	Folate studies on cultured cells from patients with the fragile X syndrome Popovich, Bradley W. (Bradley Wayne) January 1982 (has links) No description available. X chromosome -- Abnormalities. Fragile X syndrome. Mental retardation -- Genetic aspects. Folic acid -- Metabolism.

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