Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome

N Engl J Med. 1992 Jun 25;326(26):1752-5. doi: 10.1056/NEJM199206253262606.
No abstract available

Publication types

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

MeSH terms

  • Base Sequence
  • Child
  • Chromosome Deletion*
  • Female
  • Genetic Linkage
  • Humans
  • Hypogonadism / genetics*
  • Male
  • Molecular Sequence Data
  • Olfaction Disorders / genetics*
  • Syndrome
  • X Chromosome