Partial DiGeorge syndrome caused by 22q11.2 typical microdeletion without cardiac defect: report of two cases.
- Author:
Jian-Xin HE
1
;
Shen ZHANG
;
Tong-Li HAN
;
Fei-Hong YU
;
Xiu-Yun LIU
;
Bao-Ping XU
;
Kun-Ling SHEN
;
Zhai-Fang JIANG
Author Information
- Publication Type:Case Reports
- MeSH: Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; diagnosis; genetics; Humans; Infant; Male
- From: Chinese Journal of Contemporary Pediatrics 2014;16(5):541-543
- CountryChina
- Language:Chinese
