[Keratosis follicularis spinulosa decalvans (Siemens I syndrome), initial results of molecular genetic research]

Klin Monbl Augenheilkd. 1992 Dec;201(6):412-3.
[Article in German]
No abstract available

Publication types

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

MeSH terms

  • Chromosome Mapping
  • Corneal Dystrophies, Hereditary / genetics*
  • Darier Disease / genetics*
  • Genes, Dominant / genetics
  • Humans
  • Sex Chromosome Aberrations / genetics*
  • Syndrome
  • X Chromosome*