Investigation of genetic variants in patients with 22q11.2 Deletion Syndrome

被引：0
|
作者：
Ziemkiewicz, K. [1 ]
Hestand, M. S. [2 ]
Smyk, M. [1 ]
Crowley, T. B. [3 ,4 ]
Breckpot, J. [2 ]
Swillen, A. [2 ]
Kutkowska-Kazmierczak, A. [1 ]
Piotrowicz, M. [5 ]
Gieruszczak-Bialek, B. [6 ]
McDonald-McGinn, D. M. [3 ,4 ]
Vermeesch, J. R. [2 ]
Nowakowska, B. A. [1 ]
机构：
[1] Inst Mother & Child Hlth, Warsaw, Poland
[2] Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium
[3] Childrens Hosp Philadelphia, Human Genet, Philadelphia, PA 19104 USA
[4] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[5] Polish Mothers Mem Hosp Res Inst, Dept Genet, Lodz, Poland
[6] Childrens Mem Hlth Inst, Dept Med Genet, Warsaw, Poland
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26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：
P11.005A
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页码：452 / 452
页数：1
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