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

Beckwith Weidemann syndrome: a behavioral phenotype-genotype study.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 5 Oct 2008

Kent Lindsey, Bowdin Sarah, Kirby Gail A, Cooper Wendy N, Maher Eamonn R

Abstract excerpt

Neurobehavioral defects have been reported in human imprinting disorders such as Prader-Willi syndrome and Angelman syndrome and imprinted genes are often implicated in neurodevelopment processes. Beckwith-Wiedemann syndrome (BWS) is a classical human imprinting disorder characterized by prenatal...

Read the complete abstract on PubMed

Topics

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

Share to Affective Symptoms
Share to Autistic Disorder
Share to Beckwith-Wiedemann Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 11

Share to Data Collection

Share to Genomic Imprinting

Share to Mental Disorders

Share to Surveys and Questionnaires

Source

Identifiers

PMID: 18314872
DOI: 10.1002/ajmg.b.30729

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18314872-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Beckwith Weidemann syndrome: a behavioral phenotype-genotype study.PMID 18314872Read ↗

Beckwith–Wiedemann syndromeSemantic proximity Read ↗

Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromesSemantic proximity Read ↗

A neurodevelopmental survey of Angelman syndrome with genotype-phenotype correlations.Semantic proximity Read ↗

Cognitive, Social, and Emotional-Behavioral Outcomes in Children and Adolescents With Beckwith-Wiedemann Syndrome.Semantic proximity Read ↗

Molecular investigation of familial Beckwith-Wiedemann syndrome: a model for paternal imprinting.Semantic proximity Read ↗

Investigating Autism-Related Symptoms in Children with Prader-Willi Syndrome: A Case Study.Semantic proximity Read ↗

Social phenotypes in neurogenetic syndromes.Semantic proximity Read ↗

Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes.Semantic proximity Read ↗

Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues.Semantic proximity Read ↗

Delineation of behavioral phenotypes in genetic syndromes: characteristics of autism spectrum disorder, affect and hyperactivity.Semantic proximity Read ↗

Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.Semantic proximity Read ↗

Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings.Semantic proximity Read ↗

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