A case of Xp21 contiguous gene deletion syndrome: clinical and genetic study.
- Author:
Jing PENG
;
Fei YIN
;
Li-wen WU
- Publication Type:Case Reports
- MeSH: Agenesis of Corpus Callosum; Chromosomes, Human, X; Gene Deletion; Glycerol Kinase; genetics; Humans; Infant; Male; Syndrome
- From: Chinese Journal of Pediatrics 2009;47(10):792-793
- CountryChina
- Language:Chinese