Imprinting moves to the centre

This publication has 16 references indexed in Scilit:

• An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome
  Nature Genetics, 1996
• Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
  Nature Genetics, 1996
• Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors
  Human Molecular Genetics, 1996
• Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15.
  Proceedings of the National Academy of Sciences, 1996
• Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
  Nature Genetics, 1996
• Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis
  Human Molecular Genetics, 1995
• Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15
  Nature Genetics, 1995
• Beckwith-Wiedemann syndrome.
  Journal of Medical Genetics, 1994
• Genomic imprinting: control of gene expression by epigenetic inheritance
  Current Opinion in Cell Biology, 1994
• Embryological and molecular investigations of parental imprinting on mouse chromosome 7
  Nature, 1991