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

Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology.

Research in developmental disabilities - 1 Jan 2013

Sinderberry Brooke, Brown Scott, Hammond Peter, Stevens Angela F, Schall Ulrich, Murphy Declan G M, Murphy Kieran C, Campbell Linda E

Abstract excerpt

22q11.2 deletion syndrome (22q11DS) has a complex phenotype with more than 180 characteristics, including cardiac anomalies, cleft palate, intellectual disabilities, a typical facial morphology, and mental health problems. However, the variable phenotype makes it difficult to predict clinical out...

Read the complete abstract on PubMed

Topics

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

Share to Child Behavior Disorders
Share to Chromosomes, Human, Pair 22
Share to DiGeorge Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Executive Function

Share to Mental Disorders

Share to Neuropsychological Tests

Share to Social Behavior

Source

Identifiers

PMID: 22940165
DOI: 10.1016/j.ridd.2012.07.025

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-22940165-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology.PMID 22940165Read ↗

Developmental trajectories in 22q11.2 deletion syndromeSemantic proximity Read ↗

Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion SyndromeSemantic proximity Read ↗

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

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

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

22q11.2 deletion syndrome: genetics, neuroanatomy and cognitive/behavioral features keywords.Semantic proximity Read ↗

Variability in Neuropsychological Phenotypes in Patients with 22Q11.2 Deletion Syndrome: Case Series.Semantic proximity Read ↗

The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site StudySemantic proximity Read ↗

22q11 deletion syndrome: a genetic subtype of schizophrenia.Semantic proximity Read ↗

Neuroanatomical Correlates of Cognitive Dysfunction in 22q11.2 Deletion SyndromeSemantic proximity Read ↗

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion sizeSemantic proximity Read ↗

Genotype-phenotype correlation in 22q11.2 deletion syndrome.Semantic proximity Read ↗

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