Comment on

• Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene.

  Dittrich B, Buiting K, Korn B, Rickard S, Buxton J, Saitoh S, Nicholls RD, Poustka A, Winterpacht A, Zabel B, Horsthemke B. Dittrich B, et al. Nat Genet. 1996 Oct;14(2):163-70. doi: 10.1038/ng1096-163. Nat Genet. 1996. PMID: 8841186
• An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.

  Hatada I, Ohashi H, Fukushima Y, Kaneko Y, Inoue M, Komoto Y, Okada A, Ohishi S, Nabetani A, Morisaki H, Nakayama M, Niikawa N, Mukai T. Hatada I, et al. Nat Genet. 1996 Oct;14(2):171-3. doi: 10.1038/ng1096-171. Nat Genet. 1996. PMID: 8841187