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Volumn 4, Issue 4, 1997, Pages 281-289

A 3-Mb sequence-ready contig map encompassing the multiple disease gene cluster on chromosome 11q13.1-q13.3

Author keywords

BBS1; Chromosome 11; Contig; SCA5

Indexed keywords

ARTICLE; CHROMOSOME 11; CHROMOSOME MAP; GENETICS; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; MOLECULAR CLONING; MULTIGENE FAMILY; PARAGANGLIOMA; SPINOCEREBELLAR DEGENERATION; SYNDROME;

EID: 0031592730     PISSN: 13402838     EISSN: None     Source Type: Journal    
DOI: 10.1093/dnares/4.4.281     Document Type: Article
Times cited : (8)

References (11)
  • 1
    • 0021240538 scopus 로고
    • High-resolution chromosome sorting and DNA spot-blot analysis assign McArdle's syndrome to chromosome 11
    • Lebo, R. V., Gorin, F., Fletterick, R. J., Kao, F.-T., Cheung, M. C., Bruce, B. D., and Kan, Y. W. 1984, High-resolution chromosome sorting and DNA spot-blot analysis assign McArdle's syndrome to chromosome 11, Science, 225, 57-59.
    • (1984) Science , vol.225 , pp. 57-59
    • Lebo, R.V.1    Gorin, F.2    Fletterick, R.J.3    Kao, F.-T.4    Cheung, M.C.5    Bruce, B.D.6    Kan, Y.W.7
  • 2
    • 0028815440 scopus 로고
    • Defective myosin VIIA gene responsible for Usher syndrome type 1B
    • Weil, D., Blanchard, S., Kaplan, J. et al. 1995, Defective myosin VIIA gene responsible for Usher syndrome type 1B, Nature, 374, 60-61.
    • (1995) Nature , vol.374 , pp. 60-61
    • Weil, D.1    Blanchard, S.2    Kaplan, J.3
  • 3
    • 0030963446 scopus 로고    scopus 로고
    • Postional cloning of the gene for multiple endocrine neoplasia-type 1
    • Chandrasekharappa, S. C., Guru, S. C., Manickam, P. et al. 1997, Postional cloning of the gene for multiple endocrine neoplasia-type 1, Science, 276, 404-407.
    • (1997) Science , vol.276 , pp. 404-407
    • Chandrasekharappa, S.C.1    Guru, S.C.2    Manickam, P.3
  • 4
    • 0028603301 scopus 로고
    • Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci
    • Graff, C., Forsman, K., Larsson, C. et al. 1994, Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci, Genomics, 24, 425-434.
    • (1994) Genomics , vol.24 , pp. 425-434
    • Graff, C.1    Forsman, K.2    Larsson, C.3
  • 5
    • 0028979725 scopus 로고
    • Fc epsilon RI-beta polymorphism and risk of atopy in a general population sample
    • Hill, M. R., James, A. L., Faux, J. A. et al. 1995, Fc epsilon RI-beta polymorphism and risk of atopy in a general population sample, Br. Med. J., 311, 776-779.
    • (1995) Br. Med. J. , vol.311 , pp. 776-779
    • Hill, M.R.1    James, A.L.2    Faux, J.A.3
  • 6
    • 0029937085 scopus 로고    scopus 로고
    • Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13
    • Gong, Y., Vikkula, M., Boon, L. et al. 1996, Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13, Am. J. Hum. Genet., 59, 146-151.
    • (1996) Am. J. Hum. Genet. , vol.59 , pp. 146-151
    • Gong, Y.1    Vikkula, M.2    Boon, L.3
  • 7
    • 0027933734 scopus 로고
    • A genome-wide search for human type 1 diabetes susceptibility genes
    • Davies, J. L, Kawaguchi, Y., Bennett, S. T. et al. 1994, A genome-wide search for human type 1 diabetes susceptibility genes, Nature, 371, 130-136.
    • (1994) Nature , vol.371 , pp. 130-136
    • Davies, J.L.1    Kawaguchi, Y.2    Bennett, S.T.3
  • 8
    • 0028070552 scopus 로고
    • Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q
    • Hashimoto, L., Habita, C., Beressi, J. P. et al. 1994, Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q, Nature, 371, 161-164.
    • (1994) Nature , vol.371 , pp. 161-164
    • Hashimoto, L.1    Habita, C.2    Beressi, J.P.3
  • 9
    • 0028020605 scopus 로고
    • Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
    • Ranum, L. P. W., Schut, L. J., Lundgren, J. K., Orr, H. T., and Livingston, D. M. 1994, Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11, Nature Genet., 8, 280-284.
    • (1994) Nature Genet. , vol.8 , pp. 280-284
    • Ranum, L.P.W.1    Schut, L.J.2    Lundgren, J.K.3    Orr, H.T.4    Livingston, D.M.5
  • 10
    • 0028809123 scopus 로고
    • Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: Evidence for genetic heterogeneity
    • Mariman, E. C. M., van Beersum, S. E. C., Cremers, C. W. R. J., Struycken, P. M., and Ropers, H. H. 1995, Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity, Hum. Genet., 95, 56-62.
    • (1995) Hum. Genet. , vol.95 , pp. 56-62
    • Mariman, E.C.M.1    Van Beersum, S.E.C.2    Cremers, C.W.R.J.3    Struycken, P.M.4    Ropers, H.H.5
  • 11
    • 0028128537 scopus 로고
    • Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous
    • Leppert, M., Baird, L., Anderson, K. L., Otterud, B., Lupski, J. R., and Lewis, R. A. 1994, Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous, Nature Genet., 7, 108-112.
    • (1994) Nature Genet. , vol.7 , pp. 108-112
    • Leppert, M.1    Baird, L.2    Anderson, K.L.3    Otterud, B.4    Lupski, J.R.5    Lewis, R.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.