Isolated congenital anosmia locus maps to 18p11.23-q12.2

J Med Genet. 2004 Apr;41(4):299-303. doi: 10.1136/jmg.2003.015313.
No abstract available

Publication types

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

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 18*
  • Female
  • Genetic Linkage
  • Haplotypes
  • Humans
  • Male
  • Olfaction Disorders / congenital
  • Olfaction Disorders / genetics*
  • Pedigree