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Article

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

Clinical genetics - 1 Oct 2002

Webb T, Whittington J, Clarke D, Boer H, Butler J, Holland A

Abstract excerpt

A population-based cohort of people with a clinical diagnosis of Prader-Willi syndrome (PWS) was genetically assessed using molecular diagnostic methods and subsequently divided into the following genetic subtypes involving chromosome 15: 'deletion', 'disomy' and genetically negative (referred to as 'PWS-like'). The physical and behavioral characteristics of the three groups were compared in order to evaluate the...

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Chromosome Deletion
Chromosomes, Human, Pair 15
Cognition
Cohort Studies
Genomic Imprinting

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Microsatellite Repeats

Prader-Willi Syndrome

Psychomotor Performance

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Identifiers

PMID: 12372053
DOI: 10.1034/j.1399-0004.2002.620404.x

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