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Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Is 7p14.1 an orofacial cleft risk locus? Genome-wide study of copy number variation in multiple populations provides both a replication of previous studies and an alternative explanationNandita Mukhopadhyay, Eleanor E Feingold, Harrison Brand, et al.Plos One|October 3, 2012
Enamel formation genes influence enamel microhardness before and after cariogenic challengeTakehiko Shimizu, Bao Ho, Kathleen Deeley, et al.Human Genetics|May 10, 2013
Role of TRAV locus in low caries experienceJessica Briseño-Ruiz, Takehiko Shimizu, Kathleen Deeley, et al.BMC Medical Genetics|July 16, 2014
Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decayMegan L Weber, Hong-Yuan Hsin, Ersan Kalay, et al.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.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.Pageof 5