Analysis of exome data in a UK cohort of 603 patients with syndromic orofacial clefting identifies causal molecular pathways

Wilson, K; Newbury, DF; Kini, U

Kini, U (通讯作者),Univ Oxford, Hosp NHS Fdn Trust, Oxford Ctr Genom Med, Oxford OX3 7HE, England.

HUMAN MOLECULAR GENETICS, 2023; 32 (11): 1932