作者:
Huang,L. [1]
;
Jolly,L.A. [2]
;
Willis-Owen,S. [3]
;
Gardner,A. [4]
;
Kumar,R. [5]
;
Douglas,E. [6]
;
Shoubridge,C. [7]
;
Wieczorek,D. [8]
;
Tzschach,A. [9]
;
Cohen,M. [10]
;
Hackett,A. ;
Field,M. ;
Froyen,G. ;
Hu,H. ;
Haas,S.A. ;
Ropers,H.-H. ;
Kalscheuer,V.M. ;
Corbett,M.A. ;
Gecz,J.
作者单位:
Genetics and Molecular Pathology, SA Pathology, North Adelaide, SA 5006, Australia, Institute of
[1]
Kinderzentrum München, München 81377, Germany
[2]
Institut fuer Humangenetik, Universitaetsklinikum, Essen 45122, Germany
[3]
Genetics and Molecular Pathology, SA Pathology, North Adelaide, SA 5006, Australia
[4]
Genetics and Molecular Pathology, SA Pathology, North Adelaide, SA 5006, Australia, Women's and
[5]
Human Genome Laboratory, Center for Human Genetics, KU Leuven, Leuven 3000, Belgium
[6]
Genetics and Molecular Pathology, SA Pathology, North Adelaide, SA 5006, Australia, National Heart
[7]
Max Planck Institute for Molecular Genetics, Ihnestrasse 73, D-14195 Berlin, Germany
[8]
Women's and Children's Health Research Institute, North Adelaide SA 5006, Australia
[9]
Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW 2298, Australia
[10]
发布时间
2020-12-18