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3. Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. Laffargue F; Bourthoumieu S; Llanas B; Baudouin V; Lahoche A; Morin D; Bessenay L; De Parscau L; Cloarec S; Delrue MA; Taupiac E; Dizier E; Laroche C; Bahans C; Yardin C; Lacombe D; Guigonis V Arch Dis Child; 2015 Mar; 100(3):259-64. PubMed ID: 25324567 [TBL] [Abstract][Full Text] [Related]
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