A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. [electronic resource]
- American journal of human genetics Apr 2016
- 744-54 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural
1537-6605
10.1016/j.ajhg.2016.02.014 doi
Animals Case-Control Studies Cleft Palate--diagnosis DNA-Binding Proteins--genetics Disease Models, Animal Ethnicity--genetics Genetic Loci Genome-Wide Association Study Genotyping Techniques Humans Mutation, Missense Polymorphism, Single Nucleotide Risk Factors Transcription Factors--genetics Zebrafish--embryology