作者：
Antonio Tenorio-Castano, Jair [1]
;
Arias, Pedro [2]
;
Fernandez-Jaen, Alberto [3]
;
Lay-Son, Guillermo [4]
;
Bueno-Lozano, Gloria [5]
;
Bayat, Allan [6]
;
Faivre, Laurence [7]
;
Gallego, Natalia [8]
;
Ramos, Sergio [9]
;
Butler, Kameryn M. [10]
;
Morel, Chantal [11]
;
Hadjiyannakis, Stasia [12]
;
Lespinasse, James [13]
;
Tran-Mau-Them, Frederic [14]
;
Santos-Simarro, Fernando ;
Pinson, Lucile ;
Federico Martinez-Monseny, Antonio ;
O'Callaghan Cord, Maria del Mar ;
Alvarez, Sara ;
Stolerman, Elliot S. ;
Washington, Camerun ;
Ramos, Feliciano J. ;
Lapunzina, Pablo
作者单位：
Univ Zaragoza, Univ Hosp Lozano Blesa, Sch Med, Serv Paediat,Unit Clin Genet,CIBERER GCV02
[1]
Ctr Hosp Chambery, Serv Cytogenet, Chambery, France
[2]
CIBERER, Ctr Invest Biomed Red Enfermedades Raras, ISCIII, Madrid, Spain
[3]
CHU Montpellier, Dept Genet Med Malad Rares & Med Personnalisee, Montpellier, France
[4]
Greenwood Genet Ctr, Cytogenet Lab, Greenwood, SC USA
[5]
Univ Copenhagen, Hvidovre Hosp, Dept Pediat, Copenhagen, Denmark
[6]
Hosp St Joan de Deu, Clin Genet Sect, Dept Genet & Mol Med, Barcelona, Spain
[7]
Univ Ottawa, Childrens Hosp Eastern Ontario, Div Endocrinol & Metab, Ottawa, ON, Canada
[8]
Univ Hlth Network, Fred A Litwin Family Ctr Genet Med, Toronto, ON, Canada
[9]
CHU, Pole Biol, UF6254 Innovat Diagnost Genom Malad Rares Bat, Dijon, France
[10]
NIMGENETICS, Calle Anabel Segura, Madrid, Spain
[11]
Pontificia Univ Catolica Chile, Fac Med, Div Pediat, Unidad Genet, Santiago, Chile
[12]
Univ Europea Madrid, Hosp Univ Quironsalud Madrid, Madrid, Spain
[13]
Ithaca European Reference Network, Brussels, Belgium
[14]
发布时间
2021-11-26
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