BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 7842012)

  • 1. 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; 8(2):141-7. PubMed ID: 7842012
    [TBL] [Abstract][Full Text] [Related]  

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

  • 4. On the pulse of genetic cardiology.
    Schwartz K
    Nat Genet; 1994 Oct; 8(2):110-1. PubMed ID: 7842004
    [No Abstract]   [Full Text] [Related]  

  • 5. 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; 318(8):879-85. PubMed ID: 7583778
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A mutation in HERG associated with notched T waves in long QT syndrome.
    Dausse E; Berthet M; Denjoy I; André-Fouet X; Cruaud C; Bennaceur M; Fauré S; Coumel P; Schwartz K; Guicheney P
    J Mol Cell Cardiol; 1996 Aug; 28(8):1609-15. PubMed ID: 8877771
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mapping of a gene for long QT syndrome to chromosome 4q25-27.
    Schott JJ; Charpentier F; Peltier S; Foley P; Drouin E; Bouhour JB; Donnelly P; Vergnaud G; Bachner L; Moisan JP
    Am J Hum Genet; 1995 Nov; 57(5):1114-22. PubMed ID: 7485162
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Hereditary cardiac arrhythmia].
    Le Marec H; Schott JJ
    Arch Mal Coeur Vaiss; 1997 Apr; 90 Spec No 1():57-66. PubMed ID: 9238458
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
    Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of candidate genes for genotypic diagnosis in the long QT syndrome.
    Haack B; Kupka S; Ebauer M; Siemiatkowska A; Pfister M; Kwiatkowska J; Ereciński J; Limon J; Ochman K; Blin N
    J Appl Genet; 2004; 45(3):375-81. PubMed ID: 15306731
    [TBL] [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; 252(5006):704-6. PubMed ID: 1673802
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
    Wang Q; Curran ME; Splawski I; Burn TC; Millholland JM; VanRaay TJ; Shen J; Timothy KW; Vincent GM; de Jager T; Schwartz PJ; Toubin JA; Moss AJ; Atkinson DL; Landes GM; Connors TD; Keating MT
    Nat Genet; 1996 Jan; 12(1):17-23. PubMed ID: 8528244
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Alcoholism susceptibility loci: confirmation studies in a replicate sample and further mapping.
    Foroud T; Edenberg HJ; Goate A; Rice J; Flury L; Koller DL; Bierut LJ; Conneally PM; Nurnberger JI; Bucholz KK; Li TK; Hesselbrock V; Crowe R; Schuckit M; Porjesz B; Begleiter H; Reich T
    Alcohol Clin Exp Res; 2000 Jul; 24(7):933-45. PubMed ID: 10923994
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 94(4):364-6. PubMed ID: 7927330
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A family with facioscapulohumeral muscular dystrophy and hereditary long QT syndrome].
    Kimura T; Moriwaki T; Sawada J; Naka T; Hazama T; Nakata T
    Rinsho Shinkeigaku; 1997 Aug; 37(8):690-2. PubMed ID: 9404145
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A case of term mors in utero in a chromosome 11p linked long QT syndrome family.
    Desmyttere S; Bonduelle M; De Wolf D; Liebaers I; Lissens W
    Genet Couns; 1994; 5(3):289-95. PubMed ID: 7811430
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity.
    Masotti C; Oliveira KG; Poerner F; Splendore A; Souza J; Freitas Rda S; Zechi-Ceide R; Guion-Almeida ML; Passos-Bueno MR
    Eur J Hum Genet; 2008 Feb; 16(2):145-52. PubMed ID: 18000524
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
    Bruford EA; Riise R; Teague PW; Porter K; Thomson KL; Moore AT; Jay M; Warburg M; Schinzel A; Tommerup N; Tornqvist K; Rosenberg T; Patton M; Mansfield DC; Wright AF
    Genomics; 1997 Apr; 41(1):93-9. PubMed ID: 9126487
    [TBL] [Abstract][Full Text] [Related]  

  • 20. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.
    Wang Q; Shen J; Splawski I; Atkinson D; Li Z; Robinson JL; Moss AJ; Towbin JA; Keating MT
    Cell; 1995 Mar; 80(5):805-11. PubMed ID: 7889574
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.