"Liu-Liang-Chung" syndrome with multiple congenital anomalies and the distinctive craniofacial features caused by dominant ZEB2 gene gain mutation.
- Resource Type
- Case Study
- Source
- BMC Pediatrics; 9/21/2023, Vol. 23 Issue 1, p1-6, 6p
- Subject
DOMINANCE (Genetics) GENETIC mutation CONGENITAL disorders HUMAN abnormalities CONGENITAL heart disease - Language
- ISSN
- 14712431