EXT-Mutation Analysis and Loss of Heterozygosity in Sporadic and Hereditary Osteochondromas and Secondary Chondrosarcomas-Reference-Cited by-同舟云学术

EXT-Mutation Analysis and Loss of Heterozygosity in Sporadic and Hereditary Osteochondromas and Secondary Chondrosarcomas

Published:1999-09 Issue:3 Volume:65 Page:689-698
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Bovée Judith V.M.G.,Cleton-Jansen Anne-Marie,Wuyts Wim,Caethoven Goedele,Taminiau Antonie H.M.,Bakker Egbert,Van Hul Wim,Cornelisse Cees J.,Hogendoorn Pancras C.W.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference44 articles.

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

2. Tout-velu is a drosophila homologue of the putative tumour suppressor EXT1 and is needed for Hh diffusion;Bellaiche;Nature,1998

3. Bovée JVMG, Cleton-Jansen AM, Kuipers-Dykshoorn NJ, Van den Broek LJCM, Taminiau AHM, Cornelisse CJ, Hogendoorn PCW. Loss of heterozygosity and DNA ploidy point to a diverging genetic mechanism in the origin of peripheral and central chondrosarcoma. Genes Chromosomes Cancer (in press)

4. Clonal karyotypic abnormalities of the hereditary multiple exostoses chromosomal loci 8q24.1 (EXT1) and 11p11-12 (EXT2) in patients with sporadic and hereditary osteochondromas;Bridge;Cancer,1998

5. Evidence that natural selection acts on silent mutation;Conrad;Biosystems,1983

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