Exclusion of chromosome regions 6p12 and 15q11, but not chromosome region 7p11, in a German family with autosomal dominant congenital nystagmus

Genomics. 1998 Nov 15;54(1):176-7. doi: 10.1006/geno.1998.5535.
No abstract available

Publication types

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

MeSH terms

  • Chromosomes, Human, Pair 15 / genetics
  • Chromosomes, Human, Pair 6 / genetics
  • Chromosomes, Human, Pair 7 / genetics
  • Female
  • Genes, Dominant / genetics*
  • Genetic Linkage*
  • Haplotypes
  • Humans
  • Karyotyping
  • Male
  • Nystagmus, Pathologic / congenital*
  • Nystagmus, Pathologic / genetics*
  • Nystagmus, Pathologic / physiopathology
  • Pedigree