Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism-Reference-Cited by-同舟云学术

Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism

Published:2007-02-01 Issue:2 Volume:117 Page:457-463
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Pitteloud Nelly,Quinton Richard,Pearce Simon,Raivio Taneli,Acierno James,Dwyer Andrew,Plummer Lacey,Hughes Virginia,Seminara Stephanie,Cheng Yu-Zhu,Li Wei-Ping,Maccoll Gavin,Eliseenkova Anna V.,Olsen Shaun K.,Ibrahimi Omar A.,Hayes Frances J.,Boepple Paul,Hall Janet E.,Bouloux Pierre,Mohammadi Moosa,Crowley William

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference49 articles.

1. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

2. The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

3. Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome

4. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

5. Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

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