Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The behavioral phenotype of FMR1 mutations.

American journal of medical genetics. Part C, Seminars in medical genetics - 15 Nov 2010

Boyle Lia, Kaufmann Walter E

Abstract excerpt

The purpose of this article is to provide an overview of the behavioral phenotype of FMR1 mutations, including fragile X syndrome (FXS) in order to better understand the clinical involvement of individuals affected by mutations in this gene. FXS is associated with a wide range of intellectual and behavioral problems, some relatively mild and others quite severe. FXS is the most common cause of inherited...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anxiety Disorders
Share to Attention Deficit Disorder with Hyperactivity
Share to Behavior

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child Development Disorders, Pervasive

Share to Fragile X Mental Retardation Protein

Share to Fragile X Syndrome

Share to Phenotype

Source

Identifiers

PMID: 20981777
DOI: 10.1002/ajmg.c.30277

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The behavioral phenotype of FMR1 mutations.PMID 20981777Read ↗

Rare FMR1 gene mutations causing fragile X syndrome: A review.Semantic proximity Read ↗

The psychiatric presentation of fragile x: evolution of the diagnosis and treatment of the psychiatric comorbidities of fragile X syndrome.Semantic proximity Read ↗

FMR1 and Autism, an Intriguing Connection Revisited.Semantic proximity Read ↗

Modifying behavioral phenotypes in Fmr1KO mice: genetic background differences reveal autistic-like responses.Semantic proximity Read ↗

Neuroanatomical, molecular genetic, and behavioral correlates of fragile X syndrome.Semantic proximity Read ↗

Checklist assessments of FMR1 gene mutation phenotypes.Semantic proximity Read ↗

Social behavior phenotypes in fragile X syndrome, autism, and the Fmr1 knockout mouse: theoretical comment on McNaughton et al. (2008).Semantic proximity Read ↗

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

Clinical, molecular, and pharmacological aspects of FMR1 related disorders.Semantic proximity Read ↗

Fragile X syndrome: a review of clinical and molecular diagnoses.Semantic proximity Read ↗

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome.Semantic proximity Read ↗

Fragile X syndrome and fragile X-associated disordersSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.