Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype
L Faivre, V Cormier-Daire, J M Lapierre, L Colleaux, S Jacquemont, D Geneviéve, P Saunier, A Munnich, C Turleau, S Romana, M Prieur, M C De Blois, M Vekemans
Journal of Medical Genetics Aug 2002, 39 (8) 594-596; DOI: 10.1136/jmg.39.8.594