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Article

The FMR1 Premutation Phenotype and Mother-Youth Synchrony in Fragile X Syndrome.

American journal on intellectual and developmental disabilities - 1 Nov 2021

Moser Carly, Mattie Laura, Abbeduto Leonard, Klusek Jessica

Abstract excerpt

A subset of mothers who carry the FMR1 premutation may express a unique phenotype. The relationship between the FMR1 phenotype and mother-child interaction in families with fragile X-associated disorders has not been well characterized, despite the importance of high-quality mother-child interaction for child development. This study examined the association between the FMR1 phenotype and the quality of...

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Identifiers

PMID: 34700350
DOI: 10.1352/1944-7558-126.6.443
PMCID: PMC8555425

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

The FMR1 Premutation Phenotype and Mother-Youth Synchrony in Fragile X Syndrome.PMID 34700350Read ↗

Family as a Context for Child Development: Mothers with the FMR1 Premutation and Their Children with Fragile X Syndrome.Semantic proximity Read ↗

Pragmatic Language Features of Mothers With the FMR1 Premutation Are Associated With the Language Outcomes of Adolescents and Young Adults With Fragile X Syndrome.Semantic proximity Read ↗

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Co-occurring conditions associated with FMR1 gene variations: findings from a national parent survey.Semantic proximity Read ↗

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Public Health Literature Review of Fragile X Syndrome.Semantic proximity Read ↗

Impaired eye contact in the FMR1 premutation is not associated with social anxiety or the broad autism phenotype.Semantic proximity Read ↗

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