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

Expansion of an intermediate allele of the FMR1 gene in only two generations.

Clinical genetics - 1 Nov 2005

Zuñiga A, Juan J, Mila M, Guerrero A

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Child, Preschool
Share to DNA Mutational Analysis
Share to Fragile X Mental Retardation Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fragile X Syndrome

Share to FMR1 gene

Share to Pedigree

Source

Identifiers

PMID: 16207218
DOI: 10.1111/j.1399-0004.2005.00514.x

Genes

FMR1

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Expansion of an intermediate allele of the FMR1 gene in only two generations.PMID 16207218Read ↗

An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype.Semantic proximity Read ↗

A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype.Semantic proximity Read ↗

A de novo deletion in FMR1 in a patient with developmental delay.Semantic proximity Read ↗

An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals.Semantic proximity Read ↗

Fragile X syndrome phenotype with normal FMR1 gene studies.Semantic proximity Read ↗

CGG repeat expansion at FMR1 locus - A new molecular diagnostic algorithm in fragile X syndrome.Semantic proximity Read ↗

FMR1 premutation in females diagnosed with multiple sclerosis.Semantic proximity Read ↗

Apparent FMR1 allele instability in non-fragile X males.Semantic proximity Read ↗

Harms of Deception in FMR1 Premutation Genotype-Driven Recruitment.Semantic proximity Read ↗

Expansion to full mutation of a FMR1 intermediate allele over two generations.Semantic proximity Read ↗

Three new alleles encoding an apparent Kellnull phenotype.Semantic proximity Read ↗

Chromosome mapping of the Emr1 gene.Semantic proximity Read ↗

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