(Q24678862)
Statements
Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype (English)
L Faivre
J M Lapierre
S Jacquemont
D Geneviéve
P Saunier
C Turleau
M Prieur
M C De Blois
M Vekemans
scientific article