A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical region

Hum Mol Genet. 1994 Oct;3(10):1912. doi: 10.1093/hmg/3.10.1912.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • Chromosomes, Human, Pair 15*
  • DNA / genetics*
  • DNA Primers
  • DNA Transposable Elements*
  • Databases, Factual*
  • Humans
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Polymorphism, Restriction Fragment Length
  • Prader-Willi Syndrome* / genetics*
  • Sequence Deletion*

Substances

  • DNA Primers
  • DNA Transposable Elements
  • DNA