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Journal of Dental Research|October 25, 2021
Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk LocusW Awotoye, C Comnick, C Pendleton, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|September 29, 2012
Polymorphisms in the fetal progesterone receptor and a calcium-activated potassium channel isoform are associated with preterm birth in an Argentinian populationP C Mann, M E Cooper, K K Ryckman, et al.Journal of Dental Research|September 24, 2011
Genome-wide association scan for childhood caries implicates novel genesJ R Shaffer, X Wang, E Feingold, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 12, 2011
Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disordersA Butali, P A Mossey, W L Adeyemo, et al.Journal of Dental Research|July 3, 2016
Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African PopulationsL J J Gowans, W L Adeyemo, M Eshete, et al.Journal of Dental Research|September 9, 2017
Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft PalateM A Eshete, H Liu, M Li, et al.Pageof 32