Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts

Orofacial clefts (OFCs) represent a large fraction of human birth defects and are one of the most common phenotypes affected by large copy number variants (CNVs). Due to the limited number of CNV patients in individual centers, CNV analyses of a large number of OFC patients are challenging. The pres...

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Detaylı Bibliyografya
Yayımlandı:Hum Genet
Asıl Yazarlar: Conte, Federica, Oti, Martin, Dixon, Jill, Carels, Carine E. L., Rubini, Michele, Zhou, Huiqing
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Springer Berlin Heidelberg 2015
Konular:
Original Investigation
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4698300/
https://ncbi.nlm.nih.gov/pubmed/26561393
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-015-1606-x
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