作者：
Billon, Clarisse [1]
;
Molin, Arnaud [2]
;
Poirsier, Celine [3]
;
Clemenson, Alix [4]
;
Dauge, Coralie [5]
;
Grelet, Maude [6]
;
Sigaudy, Sabine [7]
;
Patrier, Sophie [8]
;
Goldenberg, Alice [9]
;
Layet, Valerie [10]
;
Tantau, Julia [11]
;
Fleury, Clemence [12]
;
Liard, Agnes [13]
;
Diguet, Alain [14]
;
Fritih, Radia [15]
;
Verspyck, Eric [16]
;
Rendu, John [17]
;
Boutaud, Lucile [18]
;
Tessier, Aude [19]
;
Thomas, Sophie [20]
;
Razavi, Ferechte ;
Achaiaa, Amale ;
Elkhartoufi, Nadia ;
Hakkakian, Leila ;
Magnin, Eglantine ;
Bole-Feysot, Christine ;
Masson, Cecile ;
Ville, Yves ;
Roth, Philippe ;
Prieur, Fabienne ;
Bessieres, Bettina ;
Bonniere, Maryse ;
Attie-Bitach, Tania
作者单位：
CHU Rouen, Lab Anat Pathol, Pavillon Jacques Delarue, Rouen, France
[1]
Normandie Univ, Dept Genet, CHU Caen Normandie, UNICAEN, Caen, France
[2]
Robert Debre Univ Hosp, Dept Pathol, Reims, France
[3]
INSERM, Bioinformat Platform, Inst Imagine, UMR 1163, Paris, France
[4]
CHU St Etienne, Serv Anat & Cytotol Pathol, St Etienne, France
[5]
CHU Reims, Dept Genet, Reims, France
[6]
Hop Necker Enfants Malad, AP HP, Serv Histol Embryol Cytogenet, Unite Embryofoetopathol, Paris
[7]
CHU Grenoble, Unite Med Genet Mol, INSERM, U1216, Grenoble, France
[8]
Rouen Univ Hosp, Dept Obstet & Gynecol, Rouen, France
[9]
Univ Hosp, Dept Pathol, Caen, France
[10]
INSERM, Genom Platform, Inst Imagine, UMR 1163, Paris, France
[11]
Grp Hosp Havre, Consultat Genet, Le Havre, France
[12]
Hop la Timone, AP HM, Pathol Dept, Marseille, France
[13]
Hop la Timone, AP HM, Dept Genet Med, Marseille, France
[14]
CHU Ch Nicolle, Serv Anat Pathol, Rouen, France
[15]
Ctr Univ Paris, Serv Obstet Maternite Chirurg Med & Imagerie Foet, Hop Necker Enfants Malad, AP HP
[16]
CHU Rouen, Dept Chirurg Infantile, Rouen, France
[17]
CHU St Etienne, Serv Genet, Hop Nord, St Etienne, France
[18]
CHU Rouen, Ctr Normand Genom & Med Personnalisee, Ctr Reference Anomalies Dev & Syndromes Malformat
[19]
Univ Paris, Imagine Inst, INSERM, UMR 1163, Paris, France
[20]
发布时间
2021-01-13
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