A novel de novo mutation of the Nipped-B-like gene in an isolated Chinese patient with Cornelia de Lange syndrome.
- Author:
Wei-zhen XU
1
;
Chun-yue CHEN
;
Xiao-ling CHEN
;
Yan ZHAO
;
Wen-ting LIU
;
Zhen-fang DU
;
Xian-ning ZHANG
Author Information
- Publication Type:Case Reports
- MeSH: Child, Preschool; De Lange Syndrome; genetics; Female; Humans; Mutation; Proteins; genetics
- From: Chinese Medical Journal 2013;126(1):191-192
- CountryChina
- Language:English
