Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate.

In conclusion, we identified a novel cleft-susceptibility locus at chromosome 3q29 with a DLG1 as a novel candidate gene for this common craniofacial anomaly.
PMID: 28926086 [PubMed - as supplied by publisher]

Source: Clinical Genetics - September 19, 2017 Category: Genetics & Stem Cells Authors: Mostowska A, Gaczkowska A, Żukowski K, Ludwig KU, Hozyasz KK, Wójcicki P, Mangold E, Böhmer AC, Heilmann-Heimbach S, Knapp M, Zadurska M, Biedziak B, Budner M, Lasota A, Daktera-Micker A, Jagodziński PP Tags: Clin Genet Source Type: research