62 related articles for article (PubMed ID: 17442914)
1. Long-QT syndrome.
Naumova AK
N Engl J Med; 2007 Apr; 356(16):1680; author reply 1680. PubMed ID: 17442914
[No Abstract] [Full Text] [Related]
2. KVLQT1, the rhythm of imprinting.
Mannens M; Wilde A
Nat Genet; 1997 Feb; 15(2):113-5. PubMed ID: 9020829
[No Abstract] [Full Text] [Related]
3. Exclusion of HRAS from long QT locus.
Roy N; Kahlem P; Dausse E; Bennaceur M; Fauré S; Weissenbach J; Komajda M; Denjoy I; Coumel P; Schwartz K
Nat Genet; 1994 Oct; 8(2):113-4. PubMed ID: 7842005
[No Abstract] [Full Text] [Related]
4. Third and long (QT).
Nat Genet; 1996 Jan; 12(1):1-2. PubMed ID: 8528237
[No Abstract] [Full Text] [Related]
5. The long-QT syndrome.
Schulze-Bahr E; Haverkamp W; Funke H
N Engl J Med; 1995 Dec; 333(26):1783-4. PubMed ID: 7491156
[No Abstract] [Full Text] [Related]
6. Molecular basis of the long-QT syndrome associated with deafness.
Splawski I; Timothy KW; Vincent GM; Atkinson DL; Keating MT
N Engl J Med; 1997 May; 336(22):1562-7. PubMed ID: 9164812
[No Abstract] [Full Text] [Related]
7. New revelations about the long-QT syndrome.
Towbin JA
N Engl J Med; 1995 Aug; 333(6):384-5. PubMed ID: 7541894
[No 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; 8(2):141-7. PubMed ID: 7842012
[TBL] [Abstract][Full Text] [Related]
9. An NsiI RFLP in the human long QT intronic transcript 1 (LIT1).
Higashimoto K; Soejima H; Yatsuki H; Katsuki T; Mukai T
J Hum Genet; 2000; 45(2):96-7. PubMed ID: 10721672
[TBL] [Abstract][Full Text] [Related]
10. 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]
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; 318(8):879-85. PubMed ID: 7583778
[TBL] [Abstract][Full Text] [Related]
12. Imprinting mutations on human chromosome 15.
Horsthemke B; Dittrich B; Buiting K
Hum Mutat; 1997; 10(5):329-37. PubMed ID: 9375847
[TBL] [Abstract][Full Text] [Related]
13. On the pulse of genetic cardiology.
Schwartz K
Nat Genet; 1994 Oct; 8(2):110-1. PubMed ID: 7842004
[No Abstract] [Full Text] [Related]
14. [Mutation analysis of a Chinese family with inherited long QT syndrome].
Du R; Yang JG; Li W; Gui L; Yuan GH; Kang CL; Ren FX; Zhang SY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):68-70. PubMed ID: 15696484
[TBL] [Abstract][Full Text] [Related]
15. [Genetic basis of sudden cardiac death].
Priori SG; Bloise R
Recenti Prog Med; 2000 Dec; 91(12):643-6. PubMed ID: 11194484
[No Abstract] [Full Text] [Related]
16. [Relationship between torsades de pointes and QT dispersion in idiopathic long QT syndrome].
Zhao F
Di Yi Jun Yi Da Xue Xue Bao; 2005 Oct; 25(10):1312-3. PubMed ID: 16234119
[TBL] [Abstract][Full Text] [Related]
17. ECG repolarization patterns in chromosome 7-linked QT syndrome (LQTS 2).
Schulze-Bahr E; Haverkamp W; Breithardt G; Funke H; Wiebusch H; Assmann G
Circulation; 1996 Nov; 94(9):2318-9. PubMed ID: 8901702
[No Abstract] [Full Text] [Related]
18. [Mutational analyses of familial long QT syndrome].
Tanaka T
Nihon Rinsho; 1998 Feb; 56(2):532-9. PubMed ID: 9503863
[No Abstract] [Full Text] [Related]
19. [Genomic imprinting and its related diseases].
Niikawa N
Tanpakushitsu Kakusan Koso; 1997 Dec; 42(16):2626-32. PubMed ID: 9404158
[No Abstract] [Full Text] [Related]
20. [Congenital long QT syndromes].
Le Marec H; Schott JJ
Arch Mal Coeur Vaiss; 1997 Jun; 90 Spec No 3():25-35. PubMed ID: 9295920
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
