Genotype–phenotype correlation in 13q13.3–q21.3 deletion

European Journal of Medical Genetics - Tập 54 - Trang e489-e494 - 2011
Lucie Tosca1,2,3, Sophie Brisset1,2, François M. Petit2,4, Corinne Metay5, Stéphanie Latour1, Benoît Lautier1, Axel Lebas6, Luc Druart7, Olivier Picone8, Anne-Elisabeth Mas9, Sophie Prévot9, Marc Tardieu6, Michel Goossens5, Gérard Tachdjian1,2,3
1AP-HP, Histologie-Embryologie-Cytogénétique, Hôpital Antoine Béclère, Clamart F-92141, France
2Université Paris Sud, Le Kremlin-Bicêtre, F-94275, France
3INSERM U935, Villejuif F-94801, France
4AP-HP, Biochimie, Hormonologie et Génétique, Hôpital Antoine Béclère, Clamart F-92141, France
5AP-HP, Plateforme de Génomique IMRB 955, Hôpital Henri Mondor, Créteil F-94010, France
6AP-HP, Neuropédiatrie, Hôpital Bicêtre, Le Kremlin-Bicêtre F-94275, France
7Biomnis, Paris F-75014, France
8AP-HP, Gynécologie Obstétrique, Hôpital Antoine Béclère, Clamart F-92141, France
9AP-HP, Anatomie Pathologique, Hôpital Antoine Béclère, Clamart F-92141, France

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