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

关键词：

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

引用

页码：452 / 452

页数：1

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