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 FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects.

Annals of human genetics - 1 Mar 2000

Gecz J

Abstract excerpt

FRAXE fragile site associated mental retardation remains unique among X-linked mental retardation phenotypes due to its very mild to borderline nature (50< IQ< 85). It is the most prevalent form of non-specific X-linked mental retardation so far delineated, with an estimated incidence of at least 1/50-100,000 males, and with more than 50 families known worldwide. The FRAXE site is within, or immediately adjacent...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Fragile Sites
Share to Chromosome Fragility
Share to Fragile X Syndrome

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Linkage

Share to Intellectual Disability

Share to Proteins

Share to Trans-Activators

Share to X Chromosome

Source

Identifiers

PMID: 11246464
DOI: 10.1017/S0003480000007983

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects.PMID 11246464Read ↗

X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms.Semantic proximity Read ↗

FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother.Semantic proximity Read ↗

Molecular characterization of FRAXE-positive subjects with mental impairement in two unrelated Italian families.Semantic proximity Read ↗

Fragile X syndrome (review).Semantic proximity Read ↗

An ‘’Omic’’ Overview of Fragile X SyndromeSemantic proximity Read ↗

FRAXA and FRAXE: new tools for the diagnosis of mental retardation.Semantic proximity Read ↗

The fragile X syndromes.Semantic proximity Read ↗

Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation.Semantic proximity Read ↗

[Monogenic causes of nonspecific X-linked mental retardation molecular aspects].Semantic proximity Read ↗

Fragile X-related protein family: a double-edged sword in neurodevelopmental disorders and cancer.Semantic proximity Read ↗

Non-syndromic X linked intellectual disability: Current knowledge in light of the recent advances in molecular and functional studies.Semantic proximity Read ↗

[Fragile X syndrome and FMR1-dependent diseases - clinical presentation, epidemiology and molecular background].Semantic proximity Read ↗

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