Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems - D'Angelo, Carla Sustek; Paz, José A. da; Kim, Chong A.; Bertola, Débora Romeo; Castro, Cláudia Irene Emílio de; Varela, Monica Castro; Koiffmann, Celia Priszkulnik (European Journal of Medical Genetics, 2006)