作者：
Singh, Sakshi [1]
;
Gupta, Aditi [2]
;
Zech, Michael [3]
;
Sigafoos, Ashley N. [4]
;
Clark, Karl J. [5]
;
Dincer, Yasemin [6]
;
Wagner, Matias [7]
;
Humberson, Jennifer B. [8]
;
Green, Sarah [9]
;
van Gassen, Koen [10]
;
Brandt, Tracy [11]
;
Schnur, Rhonda E. [12]
;
Millan, Francisca [13]
;
Si, Yue [14]
;
Mall, Volker ;
Winkelmann, Juliane ;
Gavrilova, Ralitza H. ;
Klee, Eric W. ;
Engleman, Kendra ;
Safina, Nicole P. ;
Slaugh, Rachel ;
Bryant, Emily M. ;
Tan, Wen-Hann ;
Granadillo, Jorge ;
Misra, Sunita N. ;
Schaefer, G. Bradley ;
Towner, Shelley ;
Brilstra, Eva H. ;
Koeleman, Bobby P. C.
作者单位：
GeneDx, Gaithersburg, MD USA
[1]
Tech Univ Munich, Lehrstuhl Sozialpadiat, Munich, Germany
[2]
Helmholtz Zentrum Munchen, Inst Neurogen, Munich, Germany
[3]
Mayo Clin, Ctr Individualized Med, Rochester, MN USA
[4]
Univ Missouri, Sch Med, Childrens Mercy Kansas City, Div Clin Genet, Kansas City, MO 64108 USA
[5]
Washington Univ, Sch Med, Dept Pediat, Div Genet & Genom Med, St Louis, MO 63110 USA
[6]
Ann & Robert H Lurie Childrens Hosp, Epilepsy Ctr, Chicago, IL USA
[7]
Harvard Med Sch, Boston Childrens Hosp, Dept Med, Div Genet & Gen, Boston, MA 02115 USA
[8]
Univ Arkansas Med Sci, Sect Genet & Metab, Little Rock, AR 72205 USA
[9]
Univ Virginia, Dept Pediat, Charlottesville, VA USA
[10]
Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands
[11]
Mayo Clin, Dept Biochem & Mol Biol, Rochester, MN USA
[12]
Mayo Clin, Dept Hlth Sci Res, Rochester, MN USA
[13]
Zentrum Humangenet & Lab Diagnost MVZ, Martinsried, Germany
[14]
发布时间
2022-09-10
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