Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

J Med Genet. 2000 Mar;37(3):212-5. doi: 10.1136/jmg.37.3.212.
No abstract available

Publication types

  • Letter

MeSH terms

  • Beckwith-Wiedemann Syndrome / genetics*
  • DNA Methylation
  • DNA Mutational Analysis
  • Humans
  • Insulin-Like Growth Factor II / genetics*
  • Muscle Proteins / genetics*
  • Nuclear Proteins / genetics*
  • Polymorphism, Genetic
  • RNA, Long Noncoding
  • RNA, Untranslated*

Substances

  • H19 long non-coding RNA
  • Muscle Proteins
  • NAP1L4 protein, human
  • Nuclear Proteins
  • RNA, Long Noncoding
  • RNA, Untranslated
  • Insulin-Like Growth Factor II