A familial deletion in the Prader-Willi syndrome region including the imprinting control region

Hum Mutat. 1996;8(3):288-92. doi: 10.1002/(SICI)1098-1004(1996)8:3<288::AID-HUMU18>3.0.CO;2-Z.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Blotting, Southern
  • Chromosome Mapping
  • Chromosomes, Human, Pair 15*
  • Female
  • Genetic Markers
  • Genomic Imprinting*
  • Humans
  • Male
  • Polymerase Chain Reaction
  • Prader-Willi Syndrome / genetics*
  • Sequence Deletion*

Substances

  • Genetic Markers