A prospective study highlighting the increasing role of multiple molecular diagnoses in the field of rare diseases
Caroline Racine,Camille Engel,Frederic Tran Mau-Them,Ange-Line Bruel,Antonio Vitobello,Arthur Sorlin,Anne-Sophie Denomme-Pichon,Hana Safraou,Sophie Nambot,Julian Delanne,Aurore Garde,Marie Bournez,Sebastien Moutton,Julien Thevenon, Daphnee Lehalle,Nada Houcinat,Nolwenn Jean-Marcais,Marjolaine Willems,Alain Verloes,Fanny Laffargue,Lucile Pinson,James Lespinasse,Elodie Lacaze,David Genevieve,Olivier Patat,Laetitia Lambert,Marion Gerard-Blanluet, Charlotte Benigni,Philippine Garret,Christophe Philippe,Yannis Duffourd,Laurence Faivre,Christel Thauvin-Robinet EUROPEAN JOURNAL OF HUMAN GENETICS（2022）
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