Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2

J Med Genet. 1991 Feb;28(2):143-4. doi: 10.1136/jmg.28.2.143-a.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Adult
  • Chromosome Deletion*
  • Female
  • Humans
  • Infant, Newborn
  • Microphthalmos / genetics*
  • Orbit / abnormalities
  • Pigmentation Disorders / congenital
  • Sex Chromosome Aberrations*
  • Skin Abnormalities*
  • Syndrome
  • X Chromosome*