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Items: 1 to 20 of 434

1.

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
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.

3.

[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
4.

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, et al.

Am J Hum Genet. 1995 Nov;57(5):1114-22.

5.

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
6.

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.

PMID:
7811430
7.

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
8.

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, et al.

Hum Genet. 1994 Oct;94(4):380-4.

PMID:
7927333
9.
10.

Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error?

Aksentijevich I, Gruberg L, Pras E, Balow JE Jr, Kovo M, Gazit E, Dean M, Pras M, Kastner DL.

Hum Genet. 1993 Jul;91(6):527-34.

PMID:
8340105
11.

Linkage analysis of juvenile parkinsonism to tyrosine hydroxylase gene locus on chromosome 11.

Tanaka H, Ishikawa A, Ginns EI, Miyatake T, Tsuji S.

Neurology. 1991 May;41(5):719-22.

PMID:
1674118
12.

Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome.

Barr CL, Best L, Weksberg R.

Am J Med Genet. 2001 Nov 22;104(2):120-6.

PMID:
11746041
13.

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.

14.

[Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families].

Nakahara K, Tanaka T, Nagai R, Yazaki Y, Fukushima Y, Nakamura Y.

Rinsho Byori. 1995 Apr;43(4):353-7. Japanese.

PMID:
7739116
15.

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
16.

Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome.

Wassif WS, Farnebo F, Teh BT, Moniz CF, Li FY, Harrison JD, Peters TJ, Larsson C, Harris P.

Clin Endocrinol (Oxf). 1999 Feb;50(2):191-6.

PMID:
10396361
17.

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.

18.

Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.

Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.

Br J Dermatol. 2005 Jan;152(1):29-36.

PMID:
15656797
19.

Genetic linkage heterogeneity in the fragile X syndrome.

Brown WT, Gross AC, Chan CB, Jenkins EC.

Hum Genet. 1985;71(1):11-8.

PMID:
2993154
20.

Clinical and genetical aspects of the long QT syndrome.

Wollnik B, Guicheney P.

Herz. 1994 Apr;19(2):126-32. Review.

PMID:
8194833

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