作者：
Menke, Leonie A. [1]
;
van Belzen, Martine J. [2]
;
Alders, Marielle [3]
;
Cristofoli, Francesca [4]
;
Ehmke, Nadja [5]
;
Fergelot, Patricia [6]
;
Foster, Alison [7]
;
Gerkes, Erica H. [8]
;
Hoffer, Mariette J. V. [9]
;
Horn, Denise [10]
;
Kant, Sarina G. [11]
;
Lacombe, Didier [12]
;
Leon, Eyby [13]
;
Maas, Saskia M. [14]
;
Melis, Daniela ;
Muto, Valentina ;
Park, Soo-Mi ;
Peeters, Hilde ;
Peters, Dorien J. M. ;
Pfundt, Rolph ;
van Ravenswaaij-Arts, Conny M. A. ;
Tartaglia, Marco ;
Hennekam, Raoul C. M.
作者单位：
Radboud Univ Nijmegen, Dept Human Genet, Med Ctr, Nijmegen, Netherlands
[1]
Univ Birmingham, Inst Canc & Genom Sci, Birmingham, W Midlands, England
[2]
Leiden Univ, Dept Human Genet, Med Ctr, Leiden, Netherlands
[3]
Univ Hosp Bordeaux, Dept Genet, Bordeaux, France
[4]
Univ Naples Federico II, Dept Translat Med Sci, Naples, Italy
[5]
Acad Med Ctr, Dept Clin Genet, Amsterdam, Netherlands
[6]
Acad Med Ctr, Dept Pediat, H7-238,Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[7]
Charite, Inst Med & Human Genet, Berlin, Germany
[8]
Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
[9]
Osped Pediat Bambino Gesu, Genet & Rare Dis Res Div, Rome, Italy
[10]
Leiden Univ, Dept Clin Genet, Med Ctr, Leiden, Netherlands
[11]
Katholieke Univ Leuven, Univ Hosp Leuven, Ctr Human Genet, Leuven, Belgium
[12]
Cambridge Univ Hosp, Dept Clin Genet, Cambridge, England
[13]
Childrens Natl Hlth Syst, Div Genet & Metab, Washington, DC USA
[14]
发布时间
2017-04-06
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