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Molecular Genetics & Genomic Medicine|August 25, 2018
Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial cleftsGaniyu O Oseni, Deepti Jain, Peter A Mossey, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 17, 2022
Damaging Mutations in Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft PalateWaheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, 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.
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.
Lancet (London, England)|November 29, 2017
Universal health coverage and intersectoral action for health: key messages from Disease Control Priorities, 3rd editionDean T Jamison, Ala Alwan, Charles N Mock, 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.
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