Exome Sequencing Provides Additional Evidence for the Involvement of ARHGAP29 in Mendelian Orofacial Clefting and Extends the Phenotypic Spectrum to Isolated Cleft Palate

BACKGROUND: Recent advances in genomics methodologies, in particular the availability of next-generation sequencing approaches have made it possible to identify risk loci throughout the genome, in particular the exome. In the current study, we present findings from an exome study conducted in five a...

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Detalhes bibliográficos
Publicado no:Birth Defects Res
Main Authors: Liu, Huan, Busch, Tamara, Eliason, Steven, Anand, Deepti, Bullard, Steven, Gowans, Lord J.J, Nidey, Nichole, Petrin, Aline, Augustine-Akpan, Eno-Abasi, Saadi, Irfan, Dunnwald, Martine, Lachke, Salil A., Zhu, Ying, Adeyemo, Adebowale, Amendt, Brad, Roscioli, Tony, Cornell, Robert, Murray, Jeffrey, Butali, Azeez
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5388577/
https://ncbi.nlm.nih.gov/pubmed/28029220
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.23596
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