(Q44409922)

2 December 2017

title

Mutational analysis of Hungarian patients with androgen insensitivity syndrome (English)

1 reference

2 December 2017

Mutational Analysis of Hungarian Patients with Androgen Insensitivity Syndrome (English)

1 reference

https://api.crossref.org/works/10.1515/JPEM.2003.16.3.367

26 December 2023

1 reference

1 reference

https://api.crossref.org/works/10.1515/JPEM.2003.16.3.367

26 December 2023

8

Olaf Hiort

1 reference

2 December 2017

2

Csaba Barta

1 reference

2 December 2017

Dóra Scheiber

1

1 reference

2 December 2017

Zita Halász

3

1 reference

2 December 2017

Agnes Sallai

4

1 reference

2 December 2017

Károly Rácz

5

1 reference

2 December 2017

László Ságodi

6

1 reference

2 December 2017

György Fekete

7

1 reference

2 December 2017

János Sólyom

9

1 reference

2 December 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12705360

26 December 2023

publication date

1 March 2003

1 reference

full work available at URL

2 December 2017

https://www.degruyter.com/document/doi/10.1515/JPEM.2003.16.3.367/pdf

1 reference

https://api.crossref.org/works/10.1515/JPEM.2003.16.3.367

Journal of Pediatric Endocrinology and Metabolism

26 December 2023

published in

1 reference

2 December 2017

volume

16

1 reference

2 December 2017

issue

3

1 reference

2 December 2017

page(s)

367-373

1 reference

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

2 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.3.367

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.3.367

Androgen Resistance Associated with a Mutation of the Androgen Receptor at Amino Acid 772 (Arg→Cys) Results from a Combination of Decreased Messenger Ribonucleic Acid Levels and Impairment of Receptor Function*

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.3.367

Functional characterization of naturally occurring mutant androgen receptors from subjects with complete androgen insensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.3.367

Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.3.367

Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.3.367

Complete androgen insensitivity due to mutations in the probable alpha-helical segments of the DNA-binding domain in the human androgen receptor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.3.367

Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UK

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.3.367

Molecular analysis of the androgen receptor gene in 4 patients with complete androgen insensitivity

21 January 2018

3

1 reference

https://api.crossref.org/works/10.1515/JPEM.2003.16.3.367

Molecular prenatal diagnosis of partial androgen insensitivity syndrome based on the Hind III polymorphism of the androgen receptor gene

26 December 2023

13

1 reference

https://api.crossref.org/works/10.1515/JPEM.2003.16.3.367

26 December 2023

Identifiers

1 reference

2 December 2017

1 reference