An STS from a cDNA located in the myotonic dystrophy region (DM) on human chromosome 19q13.3

Hum Mol Genet. 1992 Jun;1(3):217. doi: 10.1093/hmg/1.3.217.
No abstract available

MeSH terms

  • Base Sequence
  • Chromosome Mapping
  • Chromosomes, Human, Pair 19*
  • DNA / genetics*
  • Humans
  • Molecular Sequence Data
  • Myotonic Dystrophy / genetics*
  • Polymerase Chain Reaction
  • Sequence Tagged Sites*

Substances

  • DNA

Associated data

  • GENBANK/M88629
  • GENBANK/M88630
  • GENBANK/M88631
  • GENBANK/M88632
  • GENBANK/M88633
  • GENBANK/M88634
  • GENBANK/M88635
  • GENBANK/M88636
  • GENBANK/M88637
  • GENBANK/X62402