Showing results (301-310 of 335) with videos related to

Sort By:
Pageof 34
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 7, 2010
CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palateAriadne Letra, Renato Menezes, Margaret E Cooper, 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.
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.
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.
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.
Med (New York, N.Y.)|December 31, 2024
Sustained growth-promoting effects of vosoritide in children with achondroplasia from an ongoing phase 3 extension studyRavi Savarirayan, Melita Irving, William R Wilcox, et al.
Plos Genetics|September 30, 2025
Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft riskJenna C Carlson, Xinyi Zhang, Zeynep Erdogan-Yildirim, et al.
BMC Oral Health|July 27, 2021
Genome-Wide Association Study (GWAS) of dental caries in diverse populationsRasha N Alotaibi, Brian J Howe, Jonathan M Chernus, 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.
Pageof 34