Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323

Hum Mol Genet. 1993 Oct;2(10):1717-8. doi: 10.1093/hmg/2.10.1717.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 8 / ultrastructure*
  • Dwarfism / genetics*
  • Face / abnormalities*
  • Female
  • Genetic Markers
  • Hand Deformities, Congenital / genetics*
  • Humans
  • Male
  • Scrotum / abnormalities*
  • Syndrome
  • Translocation, Genetic*
  • X Chromosome / ultrastructure*

Substances

  • Genetic Markers