Imprinting-Mutation Mechanisms in Prader-Willi Syndrome

This publication has 55 references indexed in Scilit:

• Industrial Synthesis of (+)-cis-Methyl Dihydrojasmonate by Enantioselective Catalytic Hydrogenation; Identification of the Precatalyst [Ru((−)-Me-DuPHOS)(H)(η6-1,3,5-cyclooctatriene)](BF4)
  Angewandte Chemie International Edition in English, 2000
• Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation
  American Journal of Medical Genetics, 1997
• A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13
  American Journal of Medical Genetics, 1996
• Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
  Nature Genetics, 1996
• Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15
  Nature Genetics, 1995
• Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
  Nature Genetics, 1994
• A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11–q13) and refined localization of the SNRPN gene
  Genomics, 1993
• Characterization of a methylation imprint in the Prader — Willi syndrome chromosome region
  Human Molecular Genetics, 1993
• Modification of 15q11 — q13 DNA methylation imprints in unique Angelman and Prader — Willi patients
  Human Molecular Genetics, 1993
• Regulation of the β-globin locus
  Current Opinion in Genetics & Development, 1993