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Article

Phenotypic involvement in females with the FMR1 gene mutation.

American journal of mental retardation : AJMR - 1 May 1998

Riddle J E, Cheema A, Sobesky W E, Gardner S C, Taylor A K, Pennington B F, Hagerman R J

Abstract excerpt

Fragile X syndrome is the most common from of inherited mental retardation. Approximately half of females with the full mutation have significant cognitive deficits, whereas females with the premutation do not. Phenotypic effects seen in 281 females (IQs from 64 to 139) were analyzed. Results showed that females with the full mutation differ significantly from controls on selected anthropometric measurements,...

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Source

Identifiers

PMID: 9606468
DOI: 10.1352/0895-8017(1998)102<0590:piifwt>2.0.co;2

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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