Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes.

In Williams syndrome (WS), a deletion of approximately 1.5 Mb on one copy of chromosome 7 causes specific physical, cognitive, and behavioral abnormalities. Molecular dissection of the phenotype may be a route to identification of genes important in human cognition and behavior. Among the genes know...

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Bibliografiska uppgifter
Huvudupphovsmän: Tassabehji, M, Metcalfe, K, Karmiloff-Smith, A, Carette, M J, Grant, J, Dennis, N, Reardon, W, Splitt, M, Read, A P, Donnai, D
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1999
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377709/
https://ncbi.nlm.nih.gov/pubmed/9915950
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