Abstract
A large tuberous sclerosis multigenerational family segregating with markers on chromosome 9q from the TSC1 region was studied with a new highly polymorphic marker (designated A6) from the region. A critical affected person showed recombination with the marker, eliminating approximately 100 kilobases from the telomeric end of the critical region, which contains three genes and three to four additional exons for which the associated genes have not been delineated. This information serves to further the search for the TSC1 gene.
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- Ahlsén G., Gillberg I. C., Lindblom R., Gillberg C. Tuberous sclerosis in Western Sweden. A population study of cases with early childhood onset. Arch Neurol. 1994 Jan;51(1):76–81. doi: 10.1001/archneur.1994.00540130110018. [DOI] [PubMed] [Google Scholar]
- Fryer A. E., Chalmers A., Connor J. M., Fraser I., Povey S., Yates A. D., Yates J. R., Osborne J. P. Evidence that the gene for tuberous sclerosis is on chromosome 9. Lancet. 1987 Mar 21;1(8534):659–661. doi: 10.1016/s0140-6736(87)90416-8. [DOI] [PubMed] [Google Scholar]
- Greenspan D. S., Pasquinelli A. E. BstUI and DpnII RFLPs at the COL5A1 gene. Hum Mol Genet. 1994 Feb;3(2):385–385. doi: 10.1093/hmg/3.2.385-a. [DOI] [PubMed] [Google Scholar]
- Haines J. L., Amos J., Attwood J., Bech-Hansen N. T., Burley M., Conneally P. M., Connor J. M., Fahsold R., Flodman P., Fryer A. Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative dataset. Ann N Y Acad Sci. 1991;615:256–264. doi: 10.1111/j.1749-6632.1991.tb37767.x. [DOI] [PubMed] [Google Scholar]
- Kandt R. S., Haines J. L., Smith M., Northrup H., Gardner R. J., Short M. P., Dumars K., Roach E. S., Steingold S., Wall S. Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease. Nat Genet. 1992 Sep;2(1):37–41. doi: 10.1038/ng0992-37. [DOI] [PubMed] [Google Scholar]
- Kozman H. M., Keith T. P., Donis-Keller H., White R. L., Weissenbach J., Dean M., Vergnaud G., Kidd K., Gusella J., Royle N. J. The CEPH consortium linkage map of human chromosome 16. Genomics. 1995 Jan 1;25(1):44–58. doi: 10.1016/0888-7543(95)80108-x. [DOI] [PubMed] [Google Scholar]
- Kumar A., Wolpert C., Kandt R. S., Segal J., Pufky J., Roses A. D., Pericak-Vance M. A., Gilbert J. R. A de novo frame-shift mutation in the tuberin gene. Hum Mol Genet. 1995 Aug;4(8):1471–1472. doi: 10.1093/hmg/4.8.1471. [DOI] [PubMed] [Google Scholar]
- Kwiatkowski D. J., Henske E. P., Weimer K., Ozelius L., Gusella J. F., Haines J. Construction of a GT polymorphism map of human 9q. Genomics. 1992 Feb;12(2):229–240. doi: 10.1016/0888-7543(92)90370-8. [DOI] [PubMed] [Google Scholar]
- Martin A. O., Northrup H., Ledbetter D. H., Trask B., van den Engh G., Le Beau M. M., Beaudet A. L., Gray J. W., Sekhon G., Krassikoff N. Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysis. Am J Med Genet. 1988 Nov;31(3):643–654. doi: 10.1002/ajmg.1320310320. [DOI] [PubMed] [Google Scholar]
- Murrell J., Trofatter J., Rutter M., Cutone S., Stotler C., Rutter J., Long K., Turner A., Deaven L., Buckler A. A 500-kilobase region containing the tuberous sclerosis locus (TSC1) in a 1.7-megabase YAC and cosmid contig. Genomics. 1995 Jan 1;25(1):59–65. doi: 10.1016/0888-7543(95)80109-y. [DOI] [PubMed] [Google Scholar]
- Nellist M., Brook-Carter P. T., Connor J. M., Kwiatkowski D. J., Johnson P., Sampson J. R. Identification of markers flanking the tuberous sclerosis locus on chromosome 9 (TSC1). J Med Genet. 1993 Mar;30(3):224–227. doi: 10.1136/jmg.30.3.224. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Northrup H., Kwiatkowski D. J., Roach E. S., Dobyns W. B., Lewis R. A., Herman G. E., Rodriguez E., Jr, Daiger S. P., Blanton S. H. Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere. Am J Hum Genet. 1992 Oct;51(4):709–720. [PMC free article] [PubMed] [Google Scholar]
- Porter C. J., Nahmias J., Wolfe J., Craig I. W. Dinucleotide repeat polymorphism at the human dopamine beta-hydroxylase (DBH) locus. Nucleic Acids Res. 1992 Mar 25;20(6):1429–1429. doi: 10.1093/nar/20.6.1429. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Povey S., Armour J., Farndon P., Haines J. L., Knowles M., Olopade F., Pilz A., White J. A., Kwiatkowski D. J. Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994. Ann Hum Genet. 1994 Jul;58(Pt 3):177–250. doi: 10.1111/j.1469-1809.1994.tb01887.x. [DOI] [PubMed] [Google Scholar]
- Sampson J. R., Scahill S. J., Stephenson J. B., Mann L., Connor J. M. Genetic aspects of tuberous sclerosis in the west of Scotland. J Med Genet. 1989 Jan;26(1):28–31. doi: 10.1136/jmg.26.1.28. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shen Y., Kozman H. M., Thompson A., Phillips H. A., Holman K., Nancarrow J., Lane S., Chen L. Z., Apostolou S., Doggett N. A. A PCR-based genetic linkage map of human chromosome 16. Genomics. 1994 Jul 1;22(1):68–76. doi: 10.1006/geno.1994.1346. [DOI] [PubMed] [Google Scholar]
- Wiederholt W. C., Gomez M. R., Kurland L. T. Incidence and prevalence of tuberous sclerosis in Rochester, Minnesota, 1950 through 1982. Neurology. 1985 Apr;35(4):600–603. doi: 10.1212/wnl.35.4.600. [DOI] [PubMed] [Google Scholar]
- Xu L., Sterner C., Maheshwar M. M., Wilson P. J., Nellist M., Short P. M., Haines J. L., Sampson J. R., Ramesh V. Alternative splicing of the tuberous sclerosis 2 (TSC2) gene in human and mouse tissues. Genomics. 1995 Jun 10;27(3):475–480. doi: 10.1006/geno.1995.1079. [DOI] [PubMed] [Google Scholar]
- Yamamoto F., Clausen H., White T., Marken J., Hakomori S. Molecular genetic basis of the histo-blood group ABO system. Nature. 1990 May 17;345(6272):229–233. doi: 10.1038/345229a0. [DOI] [PubMed] [Google Scholar]