A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3

Overview of attention for article published in American Journal of Human Genetics, March 2016

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RT @Eric_Fauman: After reviewing all genome-wide associations in @gwascatalog and @uk_biobank I found one where I could pretty confidently…

After reviewing all genome-wide associations in @gwascatalog and @uk_biobank I found one where I could pretty confidently assign a causal Y or Q gene. This GWAS of cleft palate https://t.co/YUUGwGux2B https://t.co/IFatgklBHd

Variantes del gen GRHL3 confieren susceptibilidad a fisura labial no sindrómica https://t.co/j9uuGSnr4l https://t.co/QQJN6gr3Wu

RT @AJHGNews: New today! Exploring variation in GRHL3 & its contribution to cleft lip/palate: https://t.co/N7A0wRIxV2 & https://t.co/Iqc4QX…

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