作者：
Polla, Daniel L. [1]
;
Edmondson, Andrew C. [2]
;
Duvet, Sandrine [3]
;
March, Michael E. [4]
;
Sousa, Ana Berta [5]
;
Lehman, Anna [6]
;
Niyazov, Dmitriy [7]
;
van Dijk, Fleur [8]
;
Demirdas, Serwet [9]
;
van Slegtenhorst, Marjon A. [10]
;
Kievit, Anneke J. A. [11]
;
Schulz, Celine [12]
;
Armstrong, Linlea [13]
;
Bi, Xin [14]
;
Rader, Daniel J. ;
Izumi, Kosuke ;
Zackai, Elaine H. ;
de Franco, Elisa ;
Jorge, Paula ;
Huffels, Sophie C. ;
Hommersom, Marina ;
Ellard, Sian ;
Lefeber, Dirk J. ;
Santani, Avni ;
Hand, Nicholas J. ;
van Bokhoven, Hans ;
He, Miao ;
de Brouwer, Arjan P. M. ;
Causes Study
作者单位：
Dept Pathol & Lab Med,Childrens Hosp Philadelphia
[1]
Perelman Sch Med,Univ Penn
[2]
Med Ctr,Radboud Univ Nijmegen
[3]
Perel Man Sch Med,Univ Penn
[4]
Dept Pediat,Childrens Hosp Philadelphia
[5]
UMR 8576,Univ Lille
[6]
Ctr Appl Genom,Childrens Hosp Philadelphia
[7]
Hosp Santa Maria,Ctr Hosp Univ Lisboa Norte
[8]
Dept Med Genet,Univ British Columbia
[9]
Tulane Sch Med,Univ Queensland
[10]
North West Thames Reg Genet Serv,London North West Univ Healthcare NHS Trust
[11]
Dept Clin Genet,Erasmus MC
[12]
Dept Mol Genet,Royal Devon & Exeter NHS Fdn Trust
[13]
EPE,Ctr Hosp Porto
[14]
发布时间
2022-10-29
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