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Journal Abstract Search

129 related items for PubMed ID: 11196677

  • 1. Linkage analysis of a candidate region in Scandinavian sib pairs with multiple sclerosis reveals linkage to chromosome 17q.
    Larsen F, Oturai A, Ryder LP, Madsen HO, Hillert J, Fredrikson S, Sandberg-Wollheim M, Laaksonen M, Harbo HF, Sawcer S, Fugger L, Sorensen PS, Svejgaard A.
    Genes Immun; 2000 Oct; 1(7):456-9. PubMed ID: 11196677
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  • 3. Linkage analysis suggests a region of importance for multiple sclerosis in 3p14-13.
    Dai Y, Xu C, Holmberg M, Oturai A, Fredrikson S, Sandberg-Wollheim M, Laaksonen M, Spurkland A, Myhr KM, Ryder LP, Sorensen PS, Svejgaard A, Hillert J.
    Genes Immun; 2001 Dec; 2(8):451-4. PubMed ID: 11781712
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  • 5. Fine mapping of the multiple sclerosis susceptibility locus on 5p14-p12.
    Riise Stensland HM, Saarela J, Bronnikov DO, Parkkonen M, Jokiaho AJ, Palotie A, Tienari PJ, Sumelahti ML, Elovaara I, Koivisto K, Pirttilä T, Reunanen M, Sobel E, Peltonen L.
    J Neuroimmunol; 2005 Dec 30; 170(1-2):122-33. PubMed ID: 16169605
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  • 6. Linkage analysis in multiple sclerosis of chromosomal regions syntenic to experimental autoimmune disease loci.
    Xu C, Dai Y, Lorentzen JC, Dahlman I, Olsson T, Hillert J.
    Eur J Hum Genet; 2001 Jun 30; 9(6):458-63. PubMed ID: 11436128
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  • 8. Association and linkage analysis of candidate chromosomal regions in multiple sclerosis: indication of disease genes in 12q23 and 7ptr-15.
    Xu C, Dai Y, Fredrikson S, Hillert J.
    Eur J Hum Genet; 1999 Jun 30; 7(2):110-6. PubMed ID: 10196692
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  • 9. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.
    Br J Dermatol; 2005 Jan 30; 152(1):29-36. PubMed ID: 15656797
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  • 10. Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.
    Ocaka L, Zhao C, Reed JA, Ebenezer ND, Brice G, Morley T, Mehta M, O'Dowd J, Weber JL, Hardcastle AJ, Child AH.
    J Med Genet; 2008 Feb 30; 45(2):87-92. PubMed ID: 17932119
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  • 11. A genome screen for linkage in Australian sibling-pairs with multiple sclerosis.
    Ban M, Stewart GJ, Bennetts BH, Heard R, Simmons R, Maranian M, Compston A, Sawcer SJ.
    Genes Immun; 2002 Dec 30; 3(8):464-9. PubMed ID: 12486604
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  • 12. Two-locus linkage analysis in multiple sclerosis (MS).
    Tienari PJ, Terwilliger JD, Ott J, Palo J, Peltonen L.
    Genomics; 1994 Jan 15; 19(2):320-5. PubMed ID: 7514567
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  • 14. Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11.
    He B, Giedraitis V, Ligers A, Binzer M, Andersen PM, Forsgren L, Sandkuijl LA, Hillert J.
    Eur J Hum Genet; 2002 Apr 15; 10(4):271-5. PubMed ID: 12032736
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  • 15. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
    Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.
    Mol Psychiatry; 2007 Apr 15; 12(4):376-84. PubMed ID: 17179998
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  • 16. Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study.
    Sutton BS, Langefeld CD, Campbell JK, Haffner SM, Norris JM, Scherzinger AL, Wagenknecht LE, Bowden DW.
    Int J Obes (Lond); 2006 Sep 15; 30(9):1433-41. PubMed ID: 16520807
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  • 17. Empirical genomewide significance levels established by whole genome simulations.
    Sawcer S, Jones HB, Judge D, Visser F, Compston A, Goodfellow PN, Clayton D.
    Genet Epidemiol; 1997 Sep 15; 14(3):223-9. PubMed ID: 9181352
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  • 18. Exploring the dense mapping of a region of potential linkage in complex disease: an example in multiple sclerosis.
    Feakes R, Sawcer S, Chataway J, Coraddu F, Broadley S, Gray J, Jones HB, Clayton D, Goodfellow PN, Compston A.
    Genet Epidemiol; 1999 Sep 15; 17(1):51-63. PubMed ID: 10323184
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  • 19. Linkage analysis of multiple sclerosis with candidate region markers in Sardinian and Continental Italian families.
    D'Alfonso S, Nisticò L, Zavattari P, Marrosu MG, Murru R, Lai M, Massacesi L, Ballerini C, Gestri D, Salvetti M, Ristori G, Bomprezzi R, Trojano M, Liguori M, Gambi D, Quattrone A, Fruci D, Cucca F, Richiardi PM, Tosi R.
    Eur J Hum Genet; 1999 Apr 15; 7(3):377-85. PubMed ID: 10234515
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  • 20. Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11.
    Naluai AT, Nilsson S, Gudjónsdóttir AH, Louka AS, Ascher H, Ek J, Hallberg B, Samuelsson L, Kristiansson B, Martinsson T, Nerman O, Sollid LM, Wahlström J.
    Eur J Hum Genet; 2001 Dec 15; 9(12):938-44. PubMed ID: 11840196
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