A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-Like phenotype and investigation of SIM1 gene deletion in 87 patients with sindromic obesity - Varela, M. C.; Kim, C. A.; Bertola, Débora Romeo; Simões-Sato, A. Y.; Castro, C. I. E.; Koiffmann, Celia Priszkulnik (Annual Meeting of the American Society of Human Genetics, 2005)