Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segment (Q69901109)

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scientific article published on 01 July 1987

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English	Linkage analysis with RFLPs in families with androgen resistance syndromes: evidence for close linkage between the androgen receptor locus and the DXS1 segment	scientific article published on 01 July 1987

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scholarly article

1 reference

Europe PubMed Central

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6 October 2019

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

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2885254%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

author name string

P Wieacker

1

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6 October 2019

J E Griffin

2

1 reference

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6 October 2019

T Wienker

3

1 reference

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6 October 2019

J M Lopez

4

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6 October 2019

J D Wilson

5

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6 October 2019

M Breckwoldt

6

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6 October 2019

publication date

1 July 1987

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6 October 2019

1 reference

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6 October 2019

76

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6 October 2019

3

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6 October 2019

248-252

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6 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00283617

0 references

Syndrome of androgen insensitivity in man: absence of 5 alpha-dihydrotestosterone binding protein in skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FAMILIAL GYNECOMASTIA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Case of familial androgynism with severe hypospadias, gynecomastia and excessive estrogen production]

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial male pseudohermaphrodism with labial testes and partial feminization: endocrine studies and genetic aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary familial hypogonadism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked Gene for Testicular Feminization in the Mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage investigation of a large family with Reifenstein's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Androgen insensitivity as a cause of infertility in otherwise normal men

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Locus on human X chromosome for dihydrotestosterone receptor and androgen insensitivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dihydrotestosterone binding by cultured human fibroblasts. Comparison of cells from control subjects and from patients with hereditary male pseudohermaphroditism due to androgen resistance

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HEREDITARY MALE PSEUDOHERMAPHRODITISM WITH HYPOGONADISM, HYPOSPADIAS, AND GYNECOMASTIA: REIFENSTEIN'S SYNDROME

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of a mutant androgen receptor in cloned fibroblasts derived from a heterozygous carrier for the syndrome of testicular feminization

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal sex in the syndrome of testicular feminisation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testicular Feminization Associated with a Thermolabile Androgen Receptor in Cultured Human Fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2885254

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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