Constitutional mismatch repair deficiency syndrome (CMMRD): the significance of customized surveillance protocol for Lynch syndrome-related tumors in relatives at risk-a case report

被引：0
|
作者：
Bosankic, Brankica [1 ]
Cuturilo, Goran [1 ,2 ]
Petrovic, Hristina [1 ]
Mijovic, Marija [1 ]
Stojanovic, Jelena Ruml [1 ]
Miletic, Aleksandra [1 ]
机构：
[1] Univ Childrens Hosp, Dept Clin Genet, Genet Lab, Belgrade, Serbia
[2] Univ Belgrade, Fac Med, Belgrade, Serbia
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31卷
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D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
EP13.070
引用
收藏
页码：265 / 266
页数：2
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