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Article

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

American journal of medical genetics. Part A - 15 Aug 2008

Bailey Donald B, Raspa Melissa, Olmsted Murrey, Holiday David B

Abstract excerpt

Parents enrolling in a national survey of families of children with fragile X (FX) reported whether each of their children had been diagnosed or treated for developmental delay or eight conditions frequently associated with FX: attention problems, hyperactivity, aggressiveness, self-injury, autism, seizures, anxiety, or depression. This article reports results for 976 full mutation males, 259 full mutation...

Read the complete abstract on PubMed

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Share to Attention Deficit and Disruptive Behavior Disorders
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Developmental Disabilities

Share to Fragile X Mental Retardation Protein

Share to Fragile X Syndrome

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Source

Identifiers

PMID: 18570292
DOI: 10.1002/ajmg.a.32439

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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