210 related articles for article (PubMed ID: 7485162)
1. 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]
2. Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.
Towbin JA; Li H; Taggart RT; Lehmann MH; Schwartz PJ; Satler CA; Ayyagari R; Robinson JL; Moss A; Hejtmancik JF
Circulation; 1994 Dec; 90(6):2635-44. PubMed ID: 7994803
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Molecular genetics in the hereditary form of long QT syndrome].
Georgijević Milić L
Med Pregl; 2000; 53(1-2):51-4. PubMed ID: 10953551
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. [QT syndrome: new diagnostic possibilities].
Lewalter T; Englisch S; Jahr S; Schumacher B; Jung W; Hesch RD; Lüderitz B
Z Kardiol; 1998 Jul; 87(7):517-21. PubMed ID: 9744062
[TBL] [Abstract][Full Text] [Related]
8. The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene.
van den Berg MH; Wilde AA; Robles de Medina EO; Meyer H; Geelen JL; Jongbloed RJ; Wellens HJ; Geraedts JP
Hum Genet; 1997 Sep; 100(3-4):356-61. PubMed ID: 9272155
[TBL] [Abstract][Full Text] [Related]
9. [Molecular genetics of the long QT syndrome: clinical aspects].
Sepp R; Csanády M
Orv Hetil; 1999 Nov; 140(47):2633-8. PubMed ID: 10613047
[TBL] [Abstract][Full Text] [Related]
10. 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; 96(4):395-400. PubMed ID: 7557959
[TBL] [Abstract][Full Text] [Related]
11. 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; 92(10):2929-34. PubMed ID: 7586261
[TBL] [Abstract][Full Text] [Related]
12. Molecular genetic aspects of the Romano-Ward long QT syndrome.
Towbin JA
Tex Heart Inst J; 1994; 21(1):42-7. PubMed ID: 8180509
[TBL] [Abstract][Full Text] [Related]
13. Molecular genetics of long QT syndrome from genes to patients.
Wang Q; Chen Q; Li H; Towbin JA
Curr Opin Cardiol; 1997 May; 12(3):310-20. PubMed ID: 9243089
[TBL] [Abstract][Full Text] [Related]
14. 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; 94(4):380-4. PubMed ID: 7927333
[TBL] [Abstract][Full Text] [Related]
15. New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
Li H; Chen Q; Moss AJ; Robinson J; Goytia V; Perry JC; Vincent GM; Priori SG; Lehmann MH; Denfield SW; Duff D; Kaine S; Shimizu W; Schwartz PJ; Wang Q; Towbin JA
Circulation; 1998 Apr; 97(13):1264-9. PubMed ID: 9570196
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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; 88(4):245-54. PubMed ID: 10408028
[TBL] [Abstract][Full Text] [Related]
18. [Long QT syndrome].
Nakajima T; Kaneko Y; Taniguchi Y; Nagai R
Nihon Rinsho; 1996 Mar; 54(3):776-81. PubMed ID: 8904236
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndrome.
Schulze-Bahr E; Haverkamp W; Wiebusch H; Schulte H; Hördt M; Borggrefe M; Breithardt G; Assmann G; Funke H
J Mol Med (Berl); 1995 Nov; 73(11):565-9. PubMed ID: 8751140
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
