A Rare Novel Copy Number Variation of Xp22.33-p11.22 Duplication is Associated with Congenital Heart Defects.
- Author:
Juan ZHANG
;
Qing-Qing WU
1
;
Li WANG
;
Li-Juan SUN
Author Information
- Publication Type:Case Reports
- MeSH: Adult; Chromosomes, Human, Pair 22; genetics; DNA Copy Number Variations; genetics; Female; Heart Defects, Congenital; diagnosis; genetics; Humans; Trisomy; genetics
- From: Chinese Medical Journal 2015;128(20):2829-2830
- CountryChina
- Language:English
