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Case Reports
. 2002 Aug;39(8):594-6.
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 M Lapierre, L Colleaux, S Jacquemont, D Geneviéve, P Saunier, A Munnich, C Turleau, S Romana, M Prieur, M C De Blois, M Vekemans
Case Reports

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

L Faivre et al. J Med Genet. 2002 Aug.

Erratum in

  • J Med Genet. 2004 Apr;41(4):320
No abstract available

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