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Article

Ovarian Hyperstimulation Syndrome Due to a Mutation in the Follicle-Stimulating Hormone Receptor

20 Aug 2003

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12930928
DOI: 10.1056/nejmoa030064

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Ovarian Hyperstimulation Syndrome Due to a Mutation in the Follicle-Stimulating Hormone ReceptorPMID 12930928Read ↗

Ovarian hyperstimulation syndrome (OHSS) due to mutations in the follicle-stimulating hormone receptor.Semantic proximity Read ↗

Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor geneSemantic proximity Read ↗

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A Chorionic Gonadotropin–Sensitive Mutation in the Follicle-Stimulating Hormone Receptor as a Cause of Familial Gestational Spontaneous Ovarian Hyperstimulation SyndromeSemantic proximity Read ↗

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Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndromeSemantic proximity Read ↗

A Mutation in the Follicle-Stimulating Hormone Receptor as a Cause of Familial Spontaneous Ovarian Hyperstimulation SyndromeSemantic proximity Read ↗

Possible familial gestational spontaneous ovarian hyperstimulation syndrome due to mutation of FSH receptors (FGSOHS).Semantic proximity Read ↗

A Mutation in the Follicle-Stimulating Hormone Receptor as a Cause of Familial Spontaneous Ovarian Hyperstimulation SyndromeSemantic proximity Read ↗

Mutations and polymorphisms of the FSH receptor (FSHR) gene: clinical implications in female fecundity and molecular biology of FSHR protein and gene.Semantic proximity Read ↗

Follicle-stimulating hormone ligand and receptor mutations, and gonadal dysfunction.Semantic proximity Read ↗

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