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146 related items for PubMed ID: 7977384

  • 1. Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype.
    Weitkamp LR, Moss AJ, Lewis RA, Hall WJ, MacCluer JW, Schwartz PJ, Locati EH, Tzivoni D, Vincent GM, Robinson JL.
    Am J Hum Genet; 1994 Dec; 55(6):1230-41. PubMed ID: 7977384
    [Abstract] [Full Text] [Related]

  • 2. Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11.
    Keating M, Dunn C, Atkinson D, Timothy K, Vincent GM, Leppert M.
    Am J Hum Genet; 1991 Dec; 49(6):1335-9. PubMed ID: 1746560
    [Abstract] [Full Text] [Related]

  • 3. Locus heterogeneity of autosomal dominant long QT syndrome.
    Curran M, Atkinson D, Timothy K, Vincent GM, Moss AJ, Leppert M, Keating M.
    J Clin Invest; 1993 Aug; 92(2):799-803. PubMed ID: 8102381
    [Abstract] [Full Text] [Related]

  • 4. Contribution of genes of the major histocompatibility complex to susceptibility and disease phenotype in inflammatory bowel disease.
    Satsangi J, Welsh KI, Bunce M, Julier C, Farrant JM, Bell JI, Jewell DP.
    Lancet; 1996 May 04; 347(9010):1212-7. PubMed ID: 8622450
    [Abstract] [Full Text] [Related]

  • 5. Evidence of a long QT founder gene with varying phenotypic expression in South African families.
    de Jager T, Corbett CH, Badenhorst JC, Brink PA, Corfield VA.
    J Med Genet; 1996 Jul 04; 33(7):567-73. PubMed ID: 8818942
    [Abstract] [Full Text] [Related]

  • 6. Molecular genetics of long QT syndrome.
    Keating MT.
    Soc Gen Physiol Ser; 1995 Jul 04; 50():53-60. PubMed ID: 7676324
    [Abstract] [Full Text] [Related]

  • 7. HLA and leprosy: segregation and linkage study.
    Dessoukey MW, el-Shiemy S, Sallam T.
    Int J Dermatol; 1996 Apr 04; 35(4):257-64. PubMed ID: 8786183
    [Abstract] [Full Text] [Related]

  • 8. Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity.
    Jiang C, Atkinson D, Towbin JA, Splawski I, Lehmann MH, Li H, Timothy K, Taggart RT, Schwartz PJ, Vincent GM.
    Nat Genet; 1994 Oct 04; 8(2):141-7. PubMed ID: 7842012
    [Abstract] [Full Text] [Related]

  • 9. MHC susceptibility genes to IgA deficiency are located in different regions on different HLA haplotypes.
    De la Concha EG, Fernandez-Arquero M, Gual L, Vigil P, Martinez A, Urcelay E, Ferreira A, Garcia-Rodriguez MC, Fontan G.
    J Immunol; 2002 Oct 15; 169(8):4637-43. PubMed ID: 12370403
    [Abstract] [Full Text] [Related]

  • 10. The LQT syndromes--current status of molecular mechanisms.
    Schulze-Bahr E, Wedekind H, Haverkamp W, Borggrefe M, Assmann G, Breithardt G, Funke H.
    Z Kardiol; 1999 Apr 15; 88(4):245-54. PubMed ID: 10408028
    [Abstract] [Full Text] [Related]

  • 11. Readjusting the localization of long QT syndrome gene on chromosome 11p15.
    Dausse E, Denjoy I, Kahlem P, Bennaceur M, Fauré S, Weissenbach J, Coumel P, Schwartz K, Guicheney P.
    C R Acad Sci III; 1995 Aug 15; 318(8):879-85. PubMed ID: 7583778
    [Abstract] [Full Text] [Related]

  • 12. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene.
    Keating M, Atkinson D, Dunn C, Timothy K, Vincent GM, Leppert M.
    Science; 1991 May 03; 252(5006):704-6. PubMed ID: 1673802
    [Abstract] [Full Text] [Related]

  • 13. No evidence for linkage of long QT syndrome and chromosome 11p15.5 markers in a Chinese family: evidence for genetic heterogeneity.
    Ko YL, Chen SA, Tang TK, Lin JL, Chiang CE, Chen JJ, Teng MS, Chang MS, Lien WP, Wu CW.
    Hum Genet; 1994 Oct 03; 94(4):364-6. PubMed ID: 7927330
    [Abstract] [Full Text] [Related]

  • 14. Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.
    Chen Q, Zhang D, Gingell RL, Moss AJ, Napolitano C, Priori SG, Schwartz PJ, Kehoe E, Robinson JL, Schulze-Bahr E, Wang Q, Towbin JA.
    Circulation; 1999 Mar 16; 99(10):1344-7. PubMed ID: 10077519
    [Abstract] [Full Text] [Related]

  • 15. Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome.
    Satler CA, Walsh EP, Vesely MR, Plummer MH, Ginsburg GS, Jacob HJ.
    Am J Med Genet; 1996 Oct 02; 65(1):27-35. PubMed ID: 8914737
    [Abstract] [Full Text] [Related]

  • 16. Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families.
    Tanaka T, Nakahara K, Kato N, Imai T, Yamazaki T, Tomita H, Shimokawa H, Matsuhashi H, Sato N, Matsui M.
    Hum Genet; 1994 Oct 02; 94(4):380-4. PubMed ID: 7927333
    [Abstract] [Full Text] [Related]

  • 17. Contribution of the MHC class II antigens to the etiology of infantile spasm in Mexican Mestizos.
    Suastegui RA, De La Rosa G, Carranza JM, Gonzalez-Astiazaran A, Gorodezky C.
    Epilepsia; 2001 Feb 02; 42(2):210-5. PubMed ID: 11240591
    [Abstract] [Full Text] [Related]

  • 18. Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia.
    Marrosu MG, Murru R, Murru MR, Costa G, Zavattari P, Whalen M, Cocco E, Mancosu C, Schirru L, Solla E, Fadda E, Melis C, Porru I, Rolesu M, Cucca F.
    Hum Mol Genet; 2001 Dec 01; 10(25):2907-16. PubMed ID: 11741834
    [Abstract] [Full Text] [Related]

  • 19. Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant gene.
    Kainulainen K, Swan H, Miettinen H, Viitasalo M, Rovamo L, Toivonen L, Kontula K.
    Hum Genet; 1995 Oct 01; 96(4):395-400. PubMed ID: 7557959
    [Abstract] [Full Text] [Related]

  • 20. ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.
    Moss AJ, Zareba W, Benhorin J, Locati EH, Hall WJ, Robinson JL, Schwartz PJ, Towbin JA, Vincent GM, Lehmann MH.
    Circulation; 1995 Nov 15; 92(10):2929-34. PubMed ID: 7586261
    [Abstract] [Full Text] [Related]

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