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Frequency of the 7q11.23 inversion polymorphism in transmitting parents of children with Williams syndrome and in the general population does not differ between North America and Europe

Inversion of the Williams syndrome (WS) region on chromosome 7q11.23 has previously been shown to occur at a higher frequency in the transmitting parents of children with WS than in the general population, suggesting that it predisposes to the WS deletion. Frohnauer et al. recently reported that the...

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Detalhes bibliográficos
Main Authors: Morris, Colleen A, Mervis, Carolyn B, Osborne, Lucy R
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3055849/
https://ncbi.nlm.nih.gov/pubmed/21356100
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-4-7
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