Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation

Shinji Saitoh, Karin Buiting, Suzanne B. Cassidy, Jeffrey M. Conroy, Daniel J. Driscoll, James M. Gabriel, Gabriele Gillessen-Kaesbach, Christopher C. Glenn, Louise R. Greenswag, Bernhard Horsthemke, Ikuko Kondo, Katsuko Kuwajima, Norio Niikawa, Peter K. Rogan, Stuart Schwartz, James Seip, Charles A. Williams, Robert D. Nicholls^*

^*Corresponding author for this work