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Article

[GNRH1 mutation in familial hypogonadotropic hypogonadism].

Medecine sciences : M/S - 1 Oct 2009

Bouligand Jérôme, Guiochon-Mantel Anne, Young Jacques

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19849976
DOI: 10.1051/medsci/20092510791

Genes

GNRH1

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Related research

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[GNRH1 mutation in familial hypogonadotropic hypogonadism].PMID 19849976Read ↗

[Clinical and molecular genetic features of cases of isolated hypogonadotropic hypogonadism, associated with defects in GNRHR genes].Semantic proximity Read ↗

[Normosmic idiopathic hypogonadotropic hypogonadism with GnRH receptor mutation(review)].Semantic proximity Read ↗

[Congenital hypogonadotropic hypogonadism].Semantic proximity Read ↗

Molecular defects of the GNRH receptor gene in Chinese patients with idiopathic hypogonadotropic hypogonadism and the severity of hypogonadismSemantic proximity Read ↗

Identification of two compound heterozygous GNRHR mutations in two siblings with congenital hypogonadotropic hypogonadism.Semantic proximity Read ↗

GNRH1 Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature Review.Semantic proximity Read ↗

Hypogonadotropic hypogonadism and GNRH1 mutations in mice and humans.Semantic proximity Read ↗

Clinical and molecular genetics of the human GnRH receptor.Semantic proximity Read ↗

Homozygous p.R31H GNRH1 mutation and normosmic congenital hypogonadotropic hypogonadism in a patient and self-limited delayed puberty in his relatives.Semantic proximity Read ↗

[Congenital hypogonadotropic hypogonadism].Semantic proximity Read ↗

Prevalence, Phenotypic Spectrum, and Modes of Inheritance of Gonadotropin-Releasing Hormone Receptor Mutations in Idiopathic Hypogonadotropic HypogonadismSemantic proximity Read ↗

A needle in a haystack: mutations in GNRH1 as a rare cause of isolated GnRH deficiency.Semantic proximity Read ↗

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