An inherited 2q13 deletion in a patient with Marfan syndrome

被引：0
|
作者：
Rasplickova, Tereza [1 ,2 ]
Vlckova, Marketa [1 ,2 ]
Cibochova, Renata [1 ,3 ]
Cibulkova, Petra [4 ]
Indrakova, Jana [4 ]
Drabova, Jana [1 ,2 ]
Moslerova, Veronika [1 ,2 ]
Novotna, Drahuse [1 ,2 ]
Kocarek, Eduard [1 ,2 ]
机构：
[1] Charles Univ Prague, Fac Med 2, Prague, Czech Republic
[2] Univ Hosp Motol, Dept Biol & Med Genet, Prague, Czech Republic
[3] Univ Hosp Motol, Dept Neurol, Prague, Czech Republic
[4] Agel Labs, Dept Med Genet, Lab Mol Biol, Novy Jicin, Czech Republic
来源：
MOLECULAR CYTOGENETICS | 2017年 / 10卷
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
F1
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收藏
页数：1
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