1. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome;Ledbetter, D.H.; Riccardi, V.M.; Airhart, S.D.; Strobel, R.J.; Keenan, B.S.; Crawford, J.D.;N Engl J Med,1981
2. Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome;Nicholls, R.D.; Knoll, J.H.M.; Butler, M.G.; Karam, S.; Lalande, M.;Nature,1989
3. Non-reciprocal and jumping translocations of 15ql-qter in Prader-Willi syndrome;Am J Med Genet,1990
4. Types, stability and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences;Rossi, E.; Floridia, G.; Casali, M.;7 Med Genet,1993
5. The presence of interstitial telomeric sequences in constitutional chromosome abnormalities;Park, V.M.; Gustashaw, K.M.; Wathen, T.M.;Am J Hum Genet,1992