Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene

Non-syndromic cleft lip with or without cleft palate (nsCL/P) ranks among the most common human congenital malformations, and has a multifactorial background in which both exogenous and genetic risk factors act in concert. The present report describes a genome-wide association study (GWAS) involving...

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書誌詳細
出版年:Genes (Basel)
主要な著者: van Rooij, Iris ALM, Ludwig, Kerstin U, Welzenbach, Julia, Ishorst, Nina, Thonissen, Michelle, Galesloot, Tessel E, Ongkosuwito, Edwin, Bergé, Stefaan J, Aldhorae, Khalid, Rojas-Martinez, Augusto, Kiemeney, Lambertus ALM, Vermeesch, Joris Robert, Brunner, Han, Roeleveld, Nel, Devriendt, Koen, Dormaar, Titiaan, Hens, Greet, Knapp, Michael, Carels, Carine, Mangold, Elisabeth
フォーマット: Artigo
言語:Inglês
出版事項: MDPI 2019
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Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6947597/
https://ncbi.nlm.nih.gov/pubmed/31817908
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10121023
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