作者：
Zollino, Marcella [1]
;
Marangi, Giuseppe [2]
;
Ponzi, Emanuela [3]
;
Orteschi, Daniela [4]
;
Ricciardi, Stefania [5]
;
Lattante, Serena [6]
;
Murdolo, Marina [7]
;
Battaglia, Domenica [8]
;
Contaldo, Ilaria [9]
;
Mercuri, Eugenio [10]
;
Stefanini, Maria Chiara [11]
;
Caumes, Roseline [12]
;
Edery, Patrick [13]
;
Rossi, Massimiliano ;
Piccione, Maria ;
Corsello, Giovanni ;
Della Monica, Matteo ;
Scarano, Francesca ;
Priolo, Manuela ;
Gentile, Mattia ;
Zampino, Giuseppe ;
Vijzelaar, Raymon ;
Abdulrahman, Omar ;
Rauch, Anita ;
Oneda, Beatrice ;
Deardorff, Matthew A. ;
Saitta, Sulagna C. ;
Falk, Marni J. ;
Dubbs, Holly ;
Zackai, Elaine
作者单位：
Univ Mississippi, Med Ctr, Dept Pediat, Jackson, MS USA
[1]
AO Bianchi Melacrino Morelli, Genet Med, Reggio Di Calabria, Italy
[2]
Childrens Hosp Philadelphia, Div Clin Genet, Philadelphia, PA 19104 USA
[3]
Hop Necker Enfants Malad, CCA Genet, Paris, France
[4]
Univ Cattolica Sacro Cuore, Ist Pediat, I-00168 Rome, Italy
[5]
MRC Holland, Amsterdam, Netherlands
[6]
Azienda Osped G Rummo, Dipartimento Genet Med, Benevento, Italy
[7]
Hosp Civils Lyon, Hop Femme Mere Enfant, Ctr Reference Anomalies Dev, Lyon, France
[8]
Univ Zurich, Inst Med Genet, CH-8603 Schwerzenbach, Switzerland
[9]
Osped Venere, Dipartimento Materno Infantile, Genet Med, Bari, Italy
[10]
Univ Palermo, Dipartimento Materno Infantile, Palermo, Italy
[11]
Univ Cattolica Sacro Cuore, Ist Genet Med, I-00168 Rome, Italy
[12]
Univ Cattolica Sacro Cuore, Ist Neuropsichiat Infantile, I-00168 Rome, Italy
[13]
发布时间
2017-04-06
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