A new HaeIII polymorphism at the D21S13 locus

Hum Genet. 1990 Oct;85(6):671. doi: 10.1007/BF00193597.

Abstract

DNA markers in the pericentromeric region of human chromosome 21 have shown linkage to a gene for Familial Alzheimer disease (FAD; St. George Hyslop et al. 1987). The limited informativeness of probes for the loci D21S13 and D21S16 have hindered precise mapping of the FAD locus and analysis of non-allelic heterogeneity in FAD (Schellenberg et al. 1988; St. George-Hyslop et al. 1987). We recently described a new EcoRII polymorphism at the D21S13 locus that was very informative in a large FAD pedigree (Pulst et al. 1990a,b). We now report another polymorphism for the D21S13 locus that further increases the informativeness of this locus.

MeSH terms

  • Blotting, Southern
  • Chromosomes, Human, Pair 21*
  • Deoxyribonucleases, Type II Site-Specific / genetics*
  • Genetic Markers
  • Humans
  • Polymorphism, Genetic*
  • Polymorphism, Restriction Fragment Length

Substances

  • Genetic Markers
  • Deoxyribonucleases, Type II Site-Specific
  • GGCC-specific type II deoxyribonucleases