Global analysis of uniparental disomy using high density genotyping arrays

Background: Uniparental disomy (UPD), the inheritance of both copies of a chromosome from a single parent, has been identified as the cause for congenital disorders such as Silver-Russell, Prader-Willi, and Angelman syndromes. Detection of UPD has largely been performed through labour intensive scre...

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Detalhes bibliográficos
Main Authors: Bruce, S, Leinonen, R, Lindgren, C, Kivinen, K, Dahlman-Wright, K, Lipsanen-Nyman, M, Hannula-Jouppi, K, Kere, J
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2005
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735941/
https://ncbi.nlm.nih.gov/pubmed/15879501
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.032367
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