1. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome;Butler, M.G.; Meany, F.J.; Palmer, C.G.;Am Jf Med Genet,1986
2. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion;Knoll, J.H.M.; Nicholls, R.D.; Magenis, E.R.; JM, Jr, Graham; Lalande, M.;Am Med Genet,1991
3. Genetic imprinting suggested by maternal uniparental heterodisomy in nondeletion Prader-Willi syndrome;Nicholls, R.D.; Knoll, J.H.; Butler, M.G.; Karam, S.; Lalande, M.;Nature,1989
4. and clinical investigations of Prader-Willi syndrome patients;Robinson, W.P.; Bottani, A.; Yagang, X.;Am Hum Genet,1991
5. Frequency of uniparental disomy in Prader-Willi syndrome;Mascari, M.J.; Ladda, R.L.; Gottlieb, W.;N Engl Med,1992