Unmasking familial CPX by WES and identification of novel clinical signs
This study emphasiz es the importance of WES analysis in familial CLP cases, combined with deep (reverse) phenotyping in “a priori” non‐syndromic clefts.
Source: American Journal of Medical Genetics Part A - Category: Genetics & Stem Cells Authors: B énédicte Demeer,
Nicole Revencu,
Raphael Helaers,
Bernard Devauchelle,
Geneviève François,
Bénédicte Bayet,
Miikka Vikkula Tags: RESEARCH ARTICLE Source Type: research