EXOSTOSES, MULTIPLE, TYPE II

Known as: EXT2 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2016
01219992016

Papers overview

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2016
2016
Exostosin glycosyltransferase (EXT) 1 and EXT2 have been identified as causative genes in osteochondroma; however, it is not… (More)
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Highly Cited
2007
Highly Cited
2007
The exostosin (EXT) family of genes encodes glycosyltransferases involved in heparan sulfate biosynthesis. Five human members of… (More)
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Review
2001
Review
2001
Hereditary multiple exostoses (HME) is a genetically heterogeneous autosomal dominant disorder characterised by the development… (More)
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Review
2001
Review
2001
Hereditary multiple exostoses (HME) is a genetically heterogeneous autosomal dominant disorder characterised by the development… (More)
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1999
1999
OBJECTIVES To identify possible mutations in our previously cloned candidate gene for hereditary multiple exostoses type II (EXT2… (More)
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