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Article

Premature ovarian failure in a female with proximal symphalangism and Noggin mutation.

Fertility and sterility - 1 Apr 2004

Kosaki Kenjiro, Sato Seiji, Hasegawa Tomonobu, Matsuo Nobutake, Suzuki Taichi, Ogata Tsutomu

Abstract excerpt

OBJECTIVE: To report a case of premature ovarian failure (POF) and a mutation of the gene for Noggin (NOG). DESIGN: Case report. SETTING: University hospital. PATIENT(S): A 33-year-old Japanese female with POF and proximal symphalangism. INTERVENTION(S): Direct sequence analysis of the NOG gene....

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Source

Identifiers

PMID: 15066478
DOI: 10.1016/j.fertnstert.2003.08.054

Genes

NOG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15066478-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Premature ovarian failure in a female with proximal symphalangism and Noggin mutation.PMID 15066478Read ↗

Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome.Semantic proximity Read ↗

Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism.Semantic proximity Read ↗

Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.Semantic proximity Read ↗

Proximal symphalangism, hyperopia, conductive hearing impairment, and the NOG gene: 2 new mutations.Semantic proximity Read ↗

Esophageal atresia/tracheoesophageal fistula and proximal symphalangism in a patient with a NOG nonsense mutation.Semantic proximity Read ↗

Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism.Semantic proximity Read ↗

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis.Semantic proximity Read ↗

Mutational analysis of the FST gene in Chinese women with idiopathic premature ovarian failure.Semantic proximity Read ↗

Identification and association analysis of single nucleotide polymorphisms in the human noggin (NOG) gene and osteoporosis phenotypes.Semantic proximity Read ↗

Mutations in the NOG gene are commonly found in congenital stapes ankylosis with symphalangism, but not in otosclerosis.Semantic proximity Read ↗

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