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. 2002 Aug;39(8):594–596. doi: 10.1136/jmg.39.8.594

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype

L Faivre, V Cormier-Daire, J Lapierre, L Colleaux, S Jacquemont, D Genevieve, P Saunier, A Munnich, C Turleau, S Romana, M Prieur, M C De Blois, M Vekemans
PMCID: PMC1735217  PMID: 12161602

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