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Duplication of the ZIC2 gene is not associated with holoprosencephaly

Cytogenetic testing using genomic microarrays presents a clinical challenge when data regarding the phenotypic consequences of the genomic alteration are not available. We describe a chromosome 13q32.3 duplication discovered by microarray testing in a fetus with a prenatally detected apparently bala...

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Detalhes bibliográficos
Main Authors: Jobanputra, Vaidehi, Burke, Alanna, Kwame, Anyane-Yeboa, Shanmugham, Anita, Shirazi, Maryam, Brown, Stephen, Warburton, Peter E., Levy, Brynn, Warburton, Dorothy
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3715301/
https://ncbi.nlm.nih.gov/pubmed/22105922
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.34375
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