The critical region for Angelman syndrome lies between D15S122 and D15S113

This publication has 10 references indexed in Scilit:

• Angelman syndrome associated with a maternal 15q11–13 deletion of less than 200 kb
  Human Molecular Genetics, 1994
• Report of the, Second International Workshop on Human Chromosome 15 Mapping 1994
  Cytogenetic and Genome Research, 1994
• A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11–q13) and refined localization of the SNRPN gene
  Genomics, 1993
• Molecular definition of the Prader — Willi syndrome chromosome region and orientation of the SNRPN gene
  Human Molecular Genetics, 1993
• Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient
  Human Molecular Genetics, 1993
• Exclusion of the GABAA-receptor β3 subunit gene as the Angelman's syndrome gene
  The Lancet, 1993
• Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.
  Journal of Medical Genetics, 1992
• Maternal but not paternal transmission of 15q11–13–linked nondeletion Angelman syndrome leads to phenotypic expression
  Nature Genetics, 1992
• ‘Puppet’ Children A Report on Three Cases
  Developmental Medicine and Child Neurology, 1965