Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

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Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

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Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

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Item

label

Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

@en

Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

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Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

@en

Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

@nl

P1476

Reproductive endocrine phenotypes relating to CHD7 mutations in humans.

@en

P2093

William F Crowley

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P2860

Reversible congenital hypogonadotropic hypogonadism in patients with CHD7, FGFR1 or GNRHR mutations

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome

Human GnRH deficiency: a unique disease model to unravel the ontogeny of GnRH neurons

CHD7 cooperates with PBAF to control multipotent neural crest formation

Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome

Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome

Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

P304

507-515

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P31

scholarly article

P356

10.1002/AJMG.C.31585

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P433

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P478

175

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P50

Ravikumar Balasubramanian

P577

2017-11-20T00:00:00Z

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P698

29152903

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P932

5790312

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