Literature DB >> 2885254

Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segment.

P Wieacker, J E Griffin, T Wienker, J M Lopez, J D Wilson, M Breckwoldt.   

Abstract

Three families with androgen resistance syndromes--two with testicular feminization and one with Reifenstein syndrome--have been studied for linkage analysis. Using three cloned DNA sequences from the centromere region and the proximal long arm of the X chromosome (p8, pDP34, and S9, which define respectively the chromosomal segments DXS1, DXYS1, and DXS17), we found no recombination between the DXS1 locus and the mutant genes in the three families. Assuming that these disorders are the result of allelic mutations at the same locus for the androgen receptor, we can conclude that there is a close linkage between DXS1 and the androgen receptor locus, with a maximum lod score zeta = 3.5 at a recombination fraction theta = 0.0 using the LIPED program (Ott 1974).

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Year:  1987        PMID: 2885254     DOI: 10.1007/bf00283617

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  20 in total

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4.  An exonic point mutation of the androgen receptor gene in a family with complete androgen insensitivity.

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5.  Molecular basis of androgen resistance in a family with a qualitative abnormality of the androgen receptor and responsive to high-dose androgen therapy.

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Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

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9.  Identification of the Underlying Androgen Receptor Defect in the Dallas Reifenstein Family.

Authors:  Zahid Ahmad; Chao Xing; Kamaldeep Panach; Ralf Kittler; Michael J McPhaul; Jean D Wilson
Journal:  J Endocr Soc       Date:  2017-05-19
  9 in total

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