Daniel K. Sabbah
Kumasi, AH, Ghana
Last Updated: 09/26/2026
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Found 8 publications
Consensus-based Detection of Aetiologic Copy Number Variants For Syndromic Orofacial Clefts Utilising Whole Exome Sequencing of Case Parent Trios.
Journal: Research square
Published: April 10, 2026
Consensus-based detection of aetiologic copy number variants for syndromic orofacial clefts utilising whole exome sequencing of case parent trios.
Journal: BMC genomic data
Published: March 25, 2026
Whole Exome Sequencing Uncovers Genetic Syndromes Associated with Orofacial Clefts presenting with Limb abnormalities in a Sub-Saharan African cohort.
Journal: Research square
Published: January 09, 2026
Whole exome sequencing uncovers genetic syndromes and putative candidate genes underlying orofacial clefts presenting with limb abnormalities in a Sub-Saharan African cohort.
Journal: BMC medical genomics
Published: December 11, 2025
Maternal plasma folate, nutrients interactions, and the risk of orofacial clefts: A case-control study in a developing country setting.
Journal: Nutrition and health
Published: December 04, 2025
Damaging Mutations in AFDN Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate.
Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: November 17, 2022
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate.
Journal: Scientific reports
Published: November 09, 2021
Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes.
Journal: Molecular genetics & genomic medicine
Published: January 07, 2021
Showing 1-8 of 8
Last Updated: 09/26/2026