Whole-genome sequencing reveals contribution of rare and common variation to structural kidney and urinary tract malformations

被引：0

作者：

Chan, Melanie ^{[1
,2
]}

Sadeghi-Alavijeh, Omid ^{[1
]}

Stanescu, Horia ^{[1
]}

Voinescu, Catalin ^{[1
]}

van der Zanden, Loes ^{[3
]}

Woud, Sander Groen In't ^{[3
]}

Feitz, Wout ^{[4
]}

Vendrig, Lisanne ^{[5
]}

Westland, Rik ^{[5
]}

Bockenhauer, Detlef ^{[6
]}

Levine, Adam ^{[7
]}

Gale, Daniel P. ^{[1
]}

机构：

[1] UCL, Dept Renal Med, London, England

[2] Imperial Coll London, Med Res Council Lab Med Sci, London, England

[3] Radboud Univ Nijmegen, IQ Hlth, Med Ctr, Nijmegen, Netherlands

[4] Radboud Univ Nijmegen, Med Ctr, Div Pediat Urol, Nijmegen, Netherlands

[5] Univ Amsterdam, Med Ctr, Emma Childrens Hosp, Dept Pediat Nephrol, Amsterdam, Netherlands

[6] UZ Leuven, Dept Paediat Nephrol, Leuven, Belgium

[7] UCL, Dept Res Pathol, London, England

来源：

关键词：

D O I：

10.1093/ndt/gfae069.002

中图分类号：

R3 [基础医学]; R4 [临床医学];

学科分类号：

1001 ; 1002 ; 100602 ;

摘要：

1761

引用

页码：I4 / I5

页数：2