Inherited and de novo androgen receptor gene mutations: investigation of single-case families (Q34471830)

2 August 2017

title

Inherited and de novo androgen receptor gene mutations: investigation of single-case families (English)

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2 August 2017

Hiort O

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2 August 2017

Sinnecker GH

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2 August 2017

Holterhus PM

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2 August 2017

Nitsche EM

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2 August 2017

Kruse K

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2 August 2017

language of work or name

English

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publication date

1 June 1998

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The Journal of Pediatrics

2 August 2017

published in

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2 August 2017

volume

132

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2 August 2017

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2 August 2017

page(s)

939-943

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Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene

2 August 2017

cites work

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Molecular Cloning of Human and Rat Complementary DNA Encoding Androgen Receptors

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The clinical and molecular spectrum of androgen insensitivity syndromes

7 January 2021

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Detection of point mutations in the androgen receptor gene using non-isotopic single strand conformation polymorphism analysis. German Collaborative Intersex Study Group.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970387-7

A practical approach to the detection of androgen receptor gene mutations and pedigree analysis in families with x-linked androgen insensitivity.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970387-7

Androgen resistance--the clinical and molecular spectrum

7 January 2021

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The androgen receptor gene mutations database.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970387-7

10.1016/S0022-3476(98)70387-7

7 January 2021

Identifiers

DOI

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2 August 2017

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