An insertion/deletion polymorphism at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13

Hum Genet. 1994 Nov;94(5):583-4. doi: 10.1007/BF00211036.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Base Sequence
  • Chromosomes, Human, Pair 15*
  • Humans
  • Molecular Sequence Data
  • Polymorphism, Restriction Fragment Length*
  • Prader-Willi Syndrome / ethnology
  • Prader-Willi Syndrome / genetics*
  • Sequence Deletion / genetics
  • White People / genetics