Genetic counseling for isolated GnRH deficiency. - Wikidata - wikimedia - TriplyDB

Genetic counseling for isolated GnRH deficiency.

Genetic counseling for isolated GnRH deficiency.

http://www.wikidata.org/entity/Q34191671

about

Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and Future Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment.Mutations in KISS1 are not responsible for idiopathic hypogonadotropic hypogonadism in Chinese patients.Genetic risk Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism Beyond hormone replacement: quality of life in women with congenital hypogonadotropic hypogonadism.Sexuality and quality of life in congenital hypogonadisms.Spectrum of phenotype and genotype of congenital isolated hypogonadotropic hypogonadism in Asian Indians.Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life Congenital combined pituitary hormone deficiency patients have better responses to gonadotrophin-induced spermatogenesis than idiopathic hypogonadotropic hypogonadism patients.

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Genetic counseling for isolated GnRH deficiency.

http://www.wikidata.org/entity/Q34191671

description

2011 nî lūn-bûn

@nan

2011 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հունիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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name

Genetic counseling for isolated GnRH deficiency.

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Genetic counseling for isolated GnRH deficiency.

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Genetic counseling for isolated GnRH deficiency.

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type

label

Genetic counseling for isolated GnRH deficiency.

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Genetic counseling for isolated GnRH deficiency.

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Genetic counseling for isolated GnRH deficiency.

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prefLabel

Genetic counseling for isolated GnRH deficiency.

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Genetic counseling for isolated GnRH deficiency.

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Genetic counseling for isolated GnRH deficiency.

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J.MCE.2011.05.041

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Molecular and Cellular Endocrinology

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Genetic counseling for isolated GnRH deficiency.

@en

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Cassandra L Buck

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Margaret G Au

http://www.w3.org/2001/XMLSchema#string

William F Crowley

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P2860

Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2

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

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

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

Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism

The GPR54 gene as a regulator of puberty

Expanding the phenotype and genotype of female GnRH deficiency

Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood

Oligogenic basis of isolated gonadotropin-releasing hormone deficiency.

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102-109

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scholarly article

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10.1016/J.MCE.2011.05.041

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1-2

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