A New Mutation Identified by Whole Exome Sequencing in a Cornelia de Lange Syndrome Newborn.
- Author:
Hua ZHANG
1
;
Li-Ming YANG
1
;
Lu YUAN
1
;
Xin TAN
2
;
Fu-Qing ZHANG
1
Author Information
- Publication Type:Letter
- From: Chinese Medical Journal 2018;131(19):2384-2385
- CountryChina
- Language:English
