Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome (Q24657612)
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Current Data About Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
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(P1932) Ingo Kurth
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(P1932) Mustafa Tekin
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(P1932) Wolfgang Wenzel
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(P1932) James F Gusella

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(P1932) Irene Meliciani

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(P1932) Richard J Sherins

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(P1476) "Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome" (language: en)

(P2093) Hyung-Goo Kim
(P1545) 1

Fei Lan
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Soo Hyun Eom
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Gil Bu Kang
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Georg Rosenberger
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Metin Ozata
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David P Bick
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Steven L Walker
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Yang Shi
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Lawrence C Layman
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