作者:
Margot, Henri [1]
;
Boursier, Guilaine [2]
;
Duflos, Claire [3]
;
Sanchez, Elodie [4]
;
Amiel, Jeanne [5]
;
Andrau, Jean-Christophe [6]
;
Arpin, Stephanie [7]
;
Brischoux-Boucher, Elise [8]
;
Boute, Odile [9]
;
Burglen, Lydie [10]
;
Caille, Charlotte [11]
;
Capri, Yline [12]
;
Collignon, Patrick [13]
;
Conrad, Solene [14]
;
Cormier-Daire, Valerie [15]
;
Delplancq, Geoffroy [16]
;
Dieterich, Klaus [17]
;
Dollfus, Helene [18]
;
Fradin, Melanie [19]
;
Faivre, Laurence [20]
;
Fernandes, Helder [21]
;
Francannet, Christine [22]
;
Gatinois, Vincent [23]
;
Gerard, Marion [24]
;
Goldenberg, Alice [25]
;
Ghoumid, Jamal [26]
;
Grotto, Sarah [27]
;
Guerrot, Anne-Marie [28]
;
Guichet, Agnes [29]
;
Isidor, Bertrand [30]
;
Jacquemont, Marie-Line [31]
;
Julia, Sophie [32]
;
Khau Van Kien, Philippe [33]
;
Legendre, Marine ;
Le Quan Sang, K. H. ;
Leheup, Bruno ;
Lyonnet, Stanislas ;
Magry, Virginie ;
Manouvrier, Sylvie ;
Martin, Dominique ;
Morel, Godelieve ;
Munnich, Arnold ;
Naudion, Sophie ;
Odent, Sylvie ;
Perrin, Laurence ;
Petit, Florence ;
Philip, Nicole ;
Rio, Marlene ;
Robbe, Julie ;
Rossi, Massimiliano ;
Sarrazin, Elisabeth ;
Toutain, Annick ;
Van Gils, Julien ;
Vera, Gabriella ;
Verloes, Alain ;
Weber, Sacha ;
Whalen, Sandra ;
Sanlaville, Damien ;
Lacombe, Didier ;
Aladjidi, Nathalie ;
Genevieve, David
作者单位:
CHU Nancy, Serv Genet Med, Nancy, France
[1]
AP HP Pitie Salpetriere, Serv Genet Med, Paris, France
[2]
CHU Caen, Serv Genet Med, Caen, France
[3]
CHU Nice, Serv Genet Med, Nice, France
[4]
CHU Marseille, Serv Genet Med, Marseille, France
[5]
CHU Grenoble, Serv Genet Med, Grenoble, France
[6]
Paris Descartes Sorbonne Paris Cite Univ, Inst Imagine, Paris, France
[7]
Univ Tours, Serv Genet, CHU Tours, UMR 1253,iBrain,Inserm, Tours, France
[8]
Univ Lille, CHU Lille, Ctr Reference Malad Rares Anomalies Dev Nord Oues, Clin Genet Med, Lille
[9]
CHU Montpellier, Dept Informat Med, Montpellier, France
[10]
CHU Brest, Serv Genet Med, Brest, France
[11]
CHU Nantes, Serv Genet Med, Nantes, France
[12]
CHU Clermont Ferrand, Serv Genet Med, Clermont Ferrand, France
[13]
CHU Reunion, Serv Genet Med, St Pierre, France
[14]
Hop Trousseau, AP HP, Dept Genet & Embryol Med,GHUEP, Ctr Reference Malformat & Malad Congenit
[15]
CHU Toulouse, Serv Genet Med, Toulouse, France
[16]
Univ Franche Comte, Ctr Genet Humaine, Besancon, France
[17]
Univ Rennes, CHU Rennes, Serv Genet Clin, IGDR,UMR6290 CNRS, Rennes, France
[18]
Normandie Univ, UNIROUEN, U1245, F-76000 Rouen, France
[19]
CHU Dijon, Serv Genet Med, Dijon, France
[20]
CHU Bordeaux, Serv Onco Hematol Pediat, Bordeaux, France
[21]
CHU Nimes, Serv Genet Med, Nimes, France
[22]
AP HP Robert Debre, Serv Genet Med, Paris, France
[23]
CHU Angers, Serv Genet Med, Angers, France
[24]
Ctr Reference Anomalies Dev & Syndromes Malformat, St Pierre, France
[25]
CHI Toulon, Serv Genet Med, Toulon, France
[26]
CHU Bordeaux, Serv Genet Med, Bordeaux, France
[27]
Univ Montpellier, IGMM, Montpellier, France
[28]
Paris Descartes Sorbonne Paris Cite Univ, Hop Necker Enfants Malades, AP HP, Federat Genet, Paris
[29]
CHU Montpellier, Dept Genet Med Malad Rares & Med Personnalisee, Montpellier, France
[30]
CHU Strasbourg, Serv Genet Med, Strasbourg, France
[31]
CHU Lyon, Serv Genet Med, Lyon, France
[32]
CH Mans, Serv Genet Med, Le Mans, France
[33]
发布时间
2020-10-12
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Genetics in medicine
Genetics in medicine
181-188页
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