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

Narrowing the critical deletion region for autism spectrum disorders on 16p11.2.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Mar 2011

Crepel An, Steyaert Jean, De la Marche Wouter, De Wolf Veerle, Fryns Jean-Pierre, Noens Ilse, Devriendt Koen, Peeters Hilde

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 Child Development Disorders, Pervasive
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 16

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

Share to Comparative Genomic Hybridization

Share to Heterozygote

Share to Nuclear Family

Share to Pedigree

Share to Risk Factors

Source

Identifiers

PMID: 21302354
DOI: 10.1002/ajmg.b.31163

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Narrowing the critical deletion region for autism spectrum disorders on 16p11.2.PMID 21302354Read ↗

Genotype-first analysis of the 16p11.2 deletion defines a new type of "autism".Semantic proximity Read ↗

Rare and common autism risk variants converge across 16p.Semantic proximity Read ↗

Phenotypic spectrum in patients with 16p11.2 deletion: a single tertiary centre experience in Türkiye.Semantic proximity Read ↗

Chromosome 8p23.2-pter: a critical region for mental retardation, autism and epilepsy?Semantic proximity Read ↗

A clinical study of patients with pericentromeric deletion and duplication within 16p12.2-p11.2.Semantic proximity Read ↗

Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay.Semantic proximity Read ↗

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.Semantic proximity Read ↗

Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children.Semantic proximity Read ↗

Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.Semantic proximity Read ↗

8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder.Semantic proximity Read ↗

22q11 deletion syndrome in childhood onset schizophrenia: an updateSemantic proximity Read ↗

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.Semantic proximity Read ↗

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