Gene for multiple exostoses (EXT2) maps to 11(p11.2p12) and is deleted in patients with a contiguous gene syndrome

Am J Med Genet. 1998 Feb 17;75(5):538-40. doi: 10.1002/(sici)1096-8628(19980217)75:5<538::aid-ajmg17>3.0.co;2-l.
No abstract available

Publication types

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

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 11 / genetics*
  • Exostoses, Multiple Hereditary / genetics*
  • Humans
  • N-Acetylglucosaminyltransferases*
  • Proteins / genetics*

Substances

  • Proteins
  • N-Acetylglucosaminyltransferases
  • exostosin-2