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

Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype?

17 Sept 2013

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 Autism Spectrum Disorder Research
Share to Congenital heart defects research
Share to Congenital Heart Disease Studies

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 24045981
DOI: 10.1007/s10803-013-1920-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype?PMID 24045981Read ↗

Adaptive and Behavioral Phenotype in Pediatric 22q11.2 Deletion Syndrome: Characterizing a High-Risk Neurogenetic Copy Number Variant.Semantic proximity Read ↗

Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.Semantic proximity Read ↗

22q11 deletion syndrome: is that what they used to call . . . ?Semantic proximity Read ↗

Social functioning profiles in adolescents and young adults with 22q11.2 deletion syndrome: similarities and differences with typically developing individualsSemantic proximity Read ↗

Social phenotypes in neurogenetic syndromes.Semantic proximity Read ↗

Social responsiveness, an autism endophenotype: genomewide significant linkage to two regions on chromosome 8.Semantic proximity Read ↗

Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome.Semantic proximity Read ↗

[22q11.2 microdeletion].Semantic proximity Read ↗

[Chromosome 22q11 deletion syndrome and its relevance for child and adolescent psychiatry. An overview of etiology, physical symptoms, aspects of child development and psychiatric disorders].Semantic proximity Read ↗

Characterizing daily-life social interactions in adolescents and young adults with neurodevelopmental disorders: a comparison between individuals with Autism Spectrum Disorders and 22q11.2 deletion syndromeSemantic proximity Read ↗

[Social cognition in children with neurogenetic syndromes: A literature review].Semantic proximity Read ↗

[Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].Semantic proximity Read ↗

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