• Lin et al., 1998 Expression and functional analysis of mouse EXT1, a homolog of the human multiple exostosis type 1 gene.

  • Raskind et al., 1998 Evaluation of locus heterogenetity and spectrum of EXT1 mutations in hereditary multiple exostoses.

  • Shan, et al., 1998 Characterization of the human Ly-6 gene 9804 and its mapping to chromosome 8q24.3: Evidence for a Ly-6 multigene family.

  • Lin and Wells, 1997b. Localization of the human H3.3A histone gene, between D1S479 and D1S439 at the distal end of chromosome 1.

  • Ugolina, et al., 1997. Regional assignment of 64 human gene transcripts on chromosome 8.

  • Philippe, et al., 1997. Mutation Screeing of EXT1 and EXT2 genes in patients with hereditary multiple exostoses.

  • Hill, et al., 1997. Assignment of fragile site 8E (FRA8E) to human chromosome band 8q24.11 adjacent to the hereditary multiple exostoses 1 gene and two overlapping Langer-Giedion syndrome deletion endpoints.

  • Taylor et al., 1997. Cell cycle specific transcription termination within the human H3.3 gene is associated with a specific protein-DNA interaction.

  • Spicer, et al.,1997. Chromosomal localization of the human and mouse hylauronidase synthetase genes.

  • Lin and Wells, 1997. Isolation of the mouse cDNA homologous to the human EXT1 gene responsible for Hereditary Multiple Exostosis.

  • Wells et al., 1997. Identification of novel mutations in the human EXT1 tumor suppressor gene.

  • Ludecke et al., 1997. Genomic Organization and promoter structure of the Human EXT1 gene.

  • Leach et al., 1997. Report of the Third International Workshop on Human Chromosome 8 Mapping.

  • Hecht et al., 1997. Hereditary multiple exostoses: Mutational studies of familial EXT1 cases and EXTassociated malignancies.

  • Blantonet al., 1996. Hereditary multiple exostoses: Confirmation of linkage to chromosomes 8 and 11.

  • Gu, Lin & Wells, 1996. B22 ubunit of ubiquinone oxidoreductase is a candidate gene for branchio-oto-renal syndrome: Implications for other hearing loss syndromes.

  • Chen et al., 1996. An integrated physical map covering 25 cM of human chromosome 8.

  • Gu et al., 1996. Detection of a meagbase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS); Implications for mapping and cloning the BOR gene.

  • Chaffanet et al., 1996. A 3.1-Mb YAC contig within the Werner's syndrome region, on the short arm of human chromosome 8.

  • Ahn et al., 1995. Cloning the putative tumour suppressor gene for hereditary multiple exostoses (EXT1).

  • Hou et al., 1995. A YAC contig spanning the LGS region on human chromosome 8: Sublocalization of EXTI and TRPSI.

    Last Updated 8/98

    Back to WIMP home page.