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.

Authors

A H Ligon, L Potocki, L G Shaffer, D Stickens, G A Evans

PMID: 9489802
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*
Exostosin 2
Humans
N-Acetylglucosaminyltransferases*
Proteins / genetics*

Substances

Proteins
N-Acetylglucosaminyltransferases
Exostosin 2