William's syndrome: gene expression is related to parental origin and regional coordinate control

William's syndrome (WS) features a spectrum of neurocognitive and behavioral abnormalities due to a rare 1.5MB deletion that includes about 24–28 genes on chromosome band 7q11.23. Study of the expression of these genes from the single normal copy provides an opportunity to elucidate the genetic...

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Detalhes bibliográficos
Main Authors: Collette, Jeremy C, Chen, Xiao-Ning, Mills, Debra L, Galaburda, Albert M, Reiss, Allan L, Bellugi, Ursula, Korenberg, Julie R
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3556903/
https://ncbi.nlm.nih.gov/pubmed/19282872
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jhg.2009.5
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