COMBINATION OF HIRSCHSPRUNG DISEASE AND A NOVEL DEFINED MUTATION RELATED CONGENITAL ADRENAL HYPERPLASIA IN CYP21A2 GENE: CASE PRESENTATION

被引：0
|
作者：
Mengen, Eda [1 ]
Kotan, L. Damla [2 ]
Topaloglu, A. Kemal [2 ]
Yuksel, Bilgin [2 ]
机构：
[1] Ankara Childrens Hematol & Oncol Training Hosp, Ankara, Turkey
[2] Cukurova Univ, Fac Med, Adana, Turkey
来源：
HORMONE RESEARCH IN PAEDIATRICS | 2017年 / 88卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P3-110
引用
收藏
页码：432 / 432
页数：1
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