作者：
Alan,Ma [1]
;
Saira,Yousoof [2]
;
John R.,Grigg [3]
;
Maree,Flaherty [4]
;
Andre E.,Minoche [5]
;
Mark J.,Cowley [6]
;
Benjamin M.,Nash [7]
;
Gladys,Ho [8]
;
Thet,Gayagay [9]
;
Tiffany,Lai [10]
;
Elizabeth,Farnsworth ;
Emma L.,Hackett ;
Katrina,Fisk ;
Karen,Wong ;
Katherine J.,Holman ;
Gemma,Jenkins ;
Anson,Cheng ;
Frank,Martin ;
Tanya,Karaconji ;
James E.,Elder ;
Annabelle,Enriquez ;
Meredith,Wilson ;
David J.,Amor ;
Chloe A.,Stutterd ;
Benjamin,Kamien ;
John,Nelson ;
Marcel E.,Dinger ;
Bruce,Bennetts ;
Robyn V.,Jamieson
作者单位：
Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children’s Hospital at Westmead
[1]
Genetic Services of Western Australia, King Edward Memorial Hospital
[2]
Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research
[3]
Disciplines of Genomic Medicine & Child and Adolescent Health, Faculty of Medicine and Health
[4]
Eye Genetics Research Unit, The Children’s Hospital at Westmead, Save Sight Institute, Children’s
[5]
Department of Ophthalmology,The Children’s Hospital at Westmead
[6]
Department of Ophthalmology,Royal Children’s Hospital
[7]
Department of Clinical Genetics, Western Sydney Genetics Program,The Children’s Hospital at Westmead
[8]
Murdoch Children’s Research Institute and University of Melbourne
[9]
Hunter Genetics
[10]
发布时间
2022-06-23
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