Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome-Reference-Cited by-同舟云学术

Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Published:2008-10 Issue:4 Volume:83 Page:511-519
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Kim Hyung-Goo,Kurth Ingo,Lan Fei,Meliciani Irene,Wenzel Wolfgang,Eom Soo Hyun,Kang Gil Bu,Rosenberger Georg,Tekin Mustafa,Ozata Metin,Bick David P.,Sherins Richard J.,Walker Steven L.,Shi Yang,Gusella James F.,Layman Lawrence C.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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5. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome;Dode;Nat. Genet.,2003

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