Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
Comprehensive analysis of <i>de novo</i> variants across 2,497 orofacial cleft trios reveals novel genetic drivers of diseaseNehir E Kurtas, Alba Sanchis-Juan, Eren Shin, et al.
Scientific Reports|July 11, 2022
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palateWaheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 17, 2022
Damaging Mutations in <b></b> Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft PalateWaheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, et al.
Molecular Genetics & Genomic Medicine|June 20, 2020
Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndromeAzeez A Alade, Carmen J Buxo-Martinez, Peter A Mossey, et al.
Oral Diseases|June 1, 2021
Variant analyses of candidate genes in orofacial clefts in multi-ethnic populationsMary Li, Joy Olotu, Carmen J Buxo-Martinez, et al.
American Journal of Human Genetics|March 29, 2016
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3Elizabeth J Leslie, Huan Liu, Jenna C Carlson, et al.
Human Molecular Genetics|April 2, 2016
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13Elizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
Human Molecular Genetics|November 20, 2018
Genomic analyses in African populations identify novel risk loci for cleft palateAzeez Butali, Peter A Mossey, Wasiu L Adeyemo, et al.
Pageof 7