The Role of EXT1 in Nonhereditary Osteochondroma: Identification of Homozygous Deletions-Reference-Cited by-同舟云学术

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The Role of EXT1 in Nonhereditary Osteochondroma: Identification of Homozygous Deletions

Published:2007-03-06 Issue:5 Volume:99 Page:396-406
ISSN:0027-8874
Container-title:JNCI Journal of the National Cancer Institute
language:en
Short-container-title:JNCI Journal of the National Cancer Institute

Author:

Hameetman L.,Szuhai K.,Yavas A.,Knijnenburg J.,van Duin M.,van Dekken H.,Taminiau A. H. M.,Cleton-Jansen A.-M.,Bovee J. V. M. G.,Hogendoorn P. C. W.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Link

http://academic.oup.com/jnci/article-pdf/99/5/396/7689624/djk067.pdf

Reference39 articles.

1. Natural history study of hereditary multiple exostoses

2. Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)

3. Positional cloning of a gene involved in hereditary multiple exostoses

4. The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes

5. Hereditary multiple exostoses and heparan sulfate polymerization

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