Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21

Orofacial clefts (OFCs) are among the most prevalent craniofacial birth defects worldwide and create a significant public health burden. The majority of OFCs are non-syndromic, and the genetic etiology of non-syndromic OFCs is only partially determined. Here, we analyze whole genome sequence (WGS) d...

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Detalhes bibliográficos
Publicado no:Hum Genet
Main Authors: Mukhopadhyay, Nandita, Bishop, Madison, Mortillo, Michael, Chopra, Pankaj, Hetmanski, Jacqueline B., Taub, Margaret A., Moreno, Lina M., Valencia-Ramirez, Luz Consuelo, Restrepo, Claudia, Wehby, George L., Hecht, Jacqueline T., Deleyiannis, Frederic, Butali, Azeez, Weinberg, Seth M., Beaty, Terri H., Murray, Jeffrey C., Leslie, Elizabeth J., Feingold, Eleanor, Marazita, Mary L.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2019
Assuntos:
Original Investigation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6981325/
https://ncbi.nlm.nih.gov/pubmed/31848685
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-019-02099-1
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