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Article

FRAXA premutation associated with premature ovarian failure.

American journal of medical genetics - 9 Aug 1996

Vianna-Morgante A M, Costa S S, Pares A S, Verreschi I T

Abstract excerpt

A family is described in which six females in three generations experienced premature ovarian failure (POF). In three of them a FRAXA premutation was documented and the carrier status of a fourth female could be inferred, because her son had the fragile X syndrome. These findings provide further evidence for a nonrandom association between POF and the FRAXA premutation.

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Source

Identifiers

PMID: 8844084
DOI: 10.1002/(SICI)1096-8628(19960809)64:2<373::AID-AJMG28>3.0.CO;2-B

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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FRAXA premutation associated with premature ovarian failure.PMID 8844084Read ↗

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Premature ovarian failure and FRAXA premutation: Positive correlation in a Brazilian survey.Semantic proximity Read ↗

Studies of FRAXA and FRAXE in women with premature ovarian failure.Semantic proximity Read ↗

Female carriers of fragile X premutations have no increased risk for additional diseases other than premature ovarian failure.Semantic proximity Read ↗

Premature ovarian failure: a phenotypic expression of fragile X premutation.Semantic proximity Read ↗

Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry.Semantic proximity Read ↗

Serum concentrations of follicle stimulating hormone may predict premature ovarian failure in FRAXA premutation women.Semantic proximity Read ↗

Premature ovarian failure (POF) and fragile X premutation females: from POF to to fragile X carrier identification, from fragile X carrier diagnosis to POF association data.Semantic proximity Read ↗

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