Society for Craniofacial Genetics and Developmental Biology 47th Annual Meeting
Poster # tbd
Tuesday, September 10, 2024 5:00 - 8:00pm Abstract
Kelsey Robinson, Sunil K. Singh, Rachel Walkup, Dorelle V. Fawwal, Wasiu Lanre Adeyemo, Terri H. Beaty, Azeez Butali, Carmen J. Buxó, David J. Cutler, Michael P. Epstein, Brooklynn Gasser, Lord JJ Gowans, Jacqueline T. Hecht, Lina Moreno Uribe, Jeffrey C. Murray, Daryl Scott, Gary M. Shaw, Mary Ann Thomas, Seth M. Weinberg, Harrison Brand, Mary L. Marazita, Robert Lipinski, Robert A. Cornell, Elizabeth J. Leslie. Recurrent mutation N383S and rare variants in PRKCI are causal for orofacial clefting and other phenotypes.