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

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.

Pediatrics - 1 Mar 2004

Butler Merlin G, Bittel Douglas C, Kibiryeva Nataliya, Talebizadeh Zohreh, Thompson Travis

Abstract excerpt

OBJECTIVE: To determine whether phenotypic differences exist among individuals with Prader-Willi syndrome with either type I or type II deletions of chromosome 15 or maternal disomy 15 leading to a better understanding of cause and pathophysiology of this classical genetic syndrome. METHODS: We analyzed clinical, anthropometric, and behavioral data in 12 individuals (5 men, 7 women; mean age: 25.9 +/- 8.8 years)...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 15

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

Share to Mental Disorders

Share to Phenotype

Share to Prader-Willi Syndrome

Share to Uniparental Disomy

Source

Open in PubMed Open full text

Identifiers

PMID: 14993551
DOI: 10.1542/peds.113.3.565
PMCID: PMC6743499

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.PMID 14993551Read ↗

A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS.Semantic proximity Read ↗

Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An UpdateSemantic proximity Read ↗

Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.Semantic proximity Read ↗

Behavioral phenotype in adults with Prader-Willi syndrome.Semantic proximity Read ↗

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.Semantic proximity Read ↗

Prader–Willi syndrome: clinical genetics, cytogenetics and molecular biologySemantic proximity Read ↗

Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome.Semantic proximity Read ↗

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome.Semantic proximity Read ↗

Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy.Semantic proximity Read ↗

Prader-Willi-like phenotypes: a systematic review of their chromosomal abnormalities.Semantic proximity Read ↗

Health Problems in Adults with Prader–Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the LiteratureSemantic proximity Read ↗

Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.Semantic proximity Read ↗

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