Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes.
Carlson, Jenna C
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes. [electronic resource] - Genetic epidemiology 12 2017 - 887-897 p. digital
Publication Type: Journal Article
1098-2272
10.1002/gepi.22090 doi
Alleles
Brain--abnormalities
Chromosomes, Human, Pair 16
Cleft Lip--genetics
Cleft Palate--genetics
Female
Forkhead Transcription Factors--genetics
Genetic Loci
Genome-Wide Association Study
Humans
Male
Phenotype
Polymorphism, Single Nucleotide
Racial Groups--genetics
Risk Factors
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes. [electronic resource] - Genetic epidemiology 12 2017 - 887-897 p. digital
Publication Type: Journal Article
1098-2272
10.1002/gepi.22090 doi
Alleles
Brain--abnormalities
Chromosomes, Human, Pair 16
Cleft Lip--genetics
Cleft Palate--genetics
Female
Forkhead Transcription Factors--genetics
Genetic Loci
Genome-Wide Association Study
Humans
Male
Phenotype
Polymorphism, Single Nucleotide
Racial Groups--genetics
Risk Factors