New Mutations ofEXT1andEXT2Genes in German Patients with Multiple Osteochondromas-Reference-Cited by-同舟云学术

New Mutations ofEXT1andEXT2Genes in German Patients with Multiple Osteochondromas

Published:2009-05 Issue:3 Volume:73 Page:283-291
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:

Author:

Heinritz Wolfram,Hüffmeier Ulrike,Strenge Sibylle,Miterski Bianca,Zweier Christiane,Leinung Steffen,Bohring Axel,Mitulla Beate,Peters Usha,Froster Ursula G.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.2009.00508.x/fullpdf

Reference45 articles.

1. Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1);Ahn;Nat Genet,1995

2. The genotype-phenotype correlation of hereditary multiple exostoses;Alvarez;Clin Genet,2006

3. EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas;Bovee;Am J Hum Genet,1999

4. The tricho-rhino-phalangeal syndrome(s): chromosome 8 long arm deletion: is there a shortest region of overlap between reported cases? TRP I and TRP II syndromes: are they separate entities?;Buhler;Am J Med Genet,1984

5. Contribution of EXT1, EXT2, and EXTL3 to heparan sulfate chain elongation;Busse;J Biol Chem,2007

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