Associated Papers
Role of MTHFR, IRF6, PAX7 and TP63 SNPs in susceptibility to non-syndromic orofacial cleft, a candidate gene study in a Portuguese population.
Mendes J et al.
Orthodontics & Craniofacial Research, 2024
Screening of IRF6 Variants in Patients Subjected to Genetic Association Studies for Nonsyndromic Cleft Lip/Palate.
Velázquez-Aragón JA et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2021
Identification of Novel Variants in Cleft Palate-Associated Genes in Brazilian Patients With Non-syndromic Cleft Palate Only.
Machado RA et al.
Frontiers in Cell and Developmental Biology, 2021
BRCA1 and BRCA2 gene variants and nonsyndromic cleft lip/palate.
Rodriguez N et al.
Birth Defects Research, 2018
Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes.
Basha M et al.
Journal of Medical Genetics, 2018
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