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American Journal of Medical Genetics. Part A|December 25, 2018
Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial cleftsJohn R Shaffer, Jessica LeClair, Jenna C Carlson, et al.
American Journal of Medical Genetics. Part A|April 21, 2017
Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palateElizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
Molecular Genetics & Genomic Medicine|March 15, 2021
Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genesLord J J Gowans, Noura Al Dhaheri, Mary Li, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 14, 2012
Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palateTao Wu, M Daniele Fallin, Min Shi, et al.
Plos Genetics|March 24, 2015
Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palateZena T Wolf, Harrison A Brand, John R Shaffer, et al.
Scientific Reports|June 20, 2024
Rare variants analyses suggest novel cleft genes in the African populationAzeez Alade, Peter Mossey, Waheed Awotoye, et al.
American Journal of Human Genetics|December 24, 2013
Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm developmentMyriam Peyrard-Janvid, Elizabeth J Leslie, Youssef A Kousa, et al.
Lancet (London, England)|December 28, 2010
Prediction of adverse maternal outcomes in pre-eclampsia: development and validation of the fullPIERS modelPeter von Dadelszen, Beth Payne, Jing Li, et al.
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