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Items: 1 to 20 of 89

1.

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, et al.

Nat Genet. 1994 Oct;8(2):113-4. No abstract available.

PMID:
7842005
2.

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.

PMID:
7583778
3.

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.

4.

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 3;252(5006):704-6.

PMID:
1673802
5.

On the pulse of genetic cardiology.

Schwartz K.

Nat Genet. 1994 Oct;8(2):110-1. No abstract available.

PMID:
7842004
6.

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.

PMID:
7994803
7.

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, et al.

Nat Genet. 1994 Oct;8(2):141-7.

PMID:
7842012
8.

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.

9.

Evidence of genetic and phenotypic heterogeneity in the Romano-Ward syndrome.

Dean JC, Cross S, Jennings K.

J Med Genet. 1993 Nov;30(11):947-50.

10.

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.

PMID:
7927330
11.

Molecular genetic aspects of the Romano-Ward long QT syndrome.

Towbin JA.

Tex Heart Inst J. 1994;21(1):42-7. Review.

12.

The long QT syndrome: a G or not a G?

Pressler ML, Hathaway DR.

J Am Coll Cardiol. 1992 Aug;20(2):504-5. No abstract available.

13.

Third and long (QT)

[No authors listed]

Nat Genet. 1996 Jan;12(1):1-2. No abstract available.

PMID:
8528237
14.

Genetics, molecular mechanisms and management of long QT syndrome.

Wang Q, Chen Q, Towbin JA.

Ann Med. 1998 Feb;30(1):58-65. Review.

PMID:
9556090
15.

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

Verhoeven K, Van Camp G, Govaerts PJ, Balemans W, Schatteman I, Verstreken M, Van Laer L, Smith RJ, Brown MR, Van de Heyning PH, Somers T, Offeciers FE, Willems PJ.

Am J Hum Genet. 1997 May;60(5):1168-73.

16.

[Linkage analysis in a Japanese long QT syndrome family].

Akimoto K, Matsuoka R, Kasanuki H, Takao A, Monma K, Hayakawa K, Hosoda S.

Kokyu To Junkan. 1993 May;41(5):463-5. Japanese.

PMID:
8484055
17.

Molecular genetics and ventricular arrhythmias.

Moss AJ.

N Engl J Med. 1992 Sep 17;327(12):885-7. No abstract available.

PMID:
1508251
18.

The D4 dopamine receptor gene maps on 11p proximal to HRAS.

Petronis A, Van Tol HH, Lichter JB, Livak KJ, Kennedy JL.

Genomics. 1993 Oct;18(1):161-3. No abstract available.

PMID:
8276407
19.

QT interval is linked to 2 long-QT syndrome loci in normal subjects.

Busjahn A, Knoblauch H, Faulhaber HD, Boeckel T, Rosenthal M, Uhlmann R, Hoehe M, Schuster H, Luft FC.

Circulation. 1999 Jun 22;99(24):3161-4.

20.

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, et al.

Am J Hum Genet. 1994 Dec;55(6):1230-41.

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