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

Faivre, L., Cormier-Daire, V., Lapierre, J. M., Colleaux, L., Jacquemont, S., Geneviève, D., … Vekemans, M. (2002). Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype. Journal of Medical Genetics, 39(8), 594–596. https://doi.org/10.1136/jmg.39.8.594