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Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Human Genetics|October 3, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
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.
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.
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.
Genetic Epidemiology|October 3, 2018
Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial cleftsJenna C Carlson, Nichole L Nidey, Azeez Butali, et al.
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