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

Systematic screening for subtelomeric anomalies in a clinical sample of autism.

Journal of autism and developmental disorders - 1 Apr 2007

Wassink Thomas H, Losh Molly, Piven Joseph, Sheffield Val C, Ashley Elizabeth, Westin Erik R, Patil Shivanand R

Abstract excerpt

High-resolution karyotyping detects cytogenetic anomalies in 5-10% of cases of autism. Karyotyping, however, may fail to detect abnormalities of chromosome subtelomeres, which are gene rich regions prone to anomalies. We assessed whether panels of FISH probes targeted for subtelomeres could detect abnormalities beyond those identified by karyotyping in 104 individuals with Pervasive Developmental Disorders (PDDs)...

Read the complete abstract on PubMed

Topics

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

Share to Autistic Disorder
Share to Child Development Disorders, Pervasive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosome Aberrations

Share to Chromosome Banding

Share to In Situ Hybridization, Fluorescence

Share to Karyotyping

Share to Klinefelter Syndrome

Share to Telomere

Source

Identifiers

PMID: 17004120
DOI: 10.1007/s10803-006-0196-9

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

Systematic screening for subtelomeric anomalies in a clinical sample of autism.PMID 17004120Read ↗

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.Semantic proximity Read ↗

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 casesSemantic proximity Read ↗

Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes.Semantic proximity Read ↗

Chromosomal abnormalities in a clinic sample of individuals with autistic disorder.Semantic proximity Read ↗

Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.Semantic proximity Read ↗

Subtelomeric rearrangements in the mentally retarded: a comparison of detection methods.Semantic proximity Read ↗

Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation.Semantic proximity Read ↗

Subtelomeric chromosome aberrations: still a lot to learn.Semantic proximity Read ↗

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder.Semantic proximity Read ↗

Genotype-phenotype association studies of chromosome 8p inverted duplication deletion syndrome.Semantic proximity Read ↗

Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.Semantic proximity Read ↗

Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation.Semantic proximity Read ↗

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