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Items: 1 to 20 of 24

1.

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.

Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, McCabe ER, Swift M.

Circulation. 1993 Jun;87(6):1854-65.

PMID:
8504498
2.

Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

Muntoni F, Cau M, Ganau A, Congiu R, Arvedi G, Mateddu A, Marrosu MG, Cianchetti C, Realdi G, Cao A, et al.

N Engl J Med. 1993 Sep 23;329(13):921-5. No abstract available.

3.

Faster sequential genetic linkage computations.

Cottingham RW Jr, Idury RM, Schäffer AA.

Am J Hum Genet. 1993 Jul;53(1):252-63.

4.

The causes of dilated cardiomyopathy: a clinicopathologic review of 673 consecutive patients.

Kasper EK, Agema WR, Hutchins GM, Deckers JW, Hare JM, Baughman KL.

J Am Coll Cardiol. 1994 Mar 1;23(3):586-90.

5.

Avoiding recomputation in linkage analysis.

Schäffer AA, Gupta SK, Shriram K, Cottingham RW Jr.

Hum Hered. 1994 Jul-Aug;44(4):225-37.

PMID:
8056435
6.

Idiopathic dilated cardiomyopathy.

Dec GW, Fuster V.

N Engl J Med. 1994 Dec 8;331(23):1564-75. Review. No abstract available.

PMID:
7969328
7.

Molecular cloning of two human cardiac gap junction proteins, connexin40 and connexin45.

Kanter HL, Saffitz JE, Beyer EC.

J Mol Cell Cardiol. 1994 Jul;26(7):861-8.

PMID:
7966354
8.

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1.

Kass S, MacRae C, Graber HL, Sparks EA, McNamara D, Boudoulas H, Basson CT, Baker PB 3rd, Cody RJ, Fishman MC, et al.

Nat Genet. 1994 Aug;7(4):546-51.

PMID:
7951328
9.

Report and abstracts of the fifth international workshop on human chromosome 3 mapping 1994. Ann Arbor, Michigan, May 8-9, 1994.

Smith DI, Glover TW, Gemmill R, Drabkin H, O'Connell P, Naylor SL.

Cytogenet Cell Genet. 1995;68(3-4):125-46. No abstract available.

PMID:
7842730
10.

Familial dilated cardiomyopathy in the United Kingdom.

Keeling PJ, Gang Y, Smith G, Seo H, Bent SE, Murday V, Caforio AL, McKenna WJ.

Br Heart J. 1995 May;73(5):417-21.

11.

Prevalence of arrhythmias in patients with idiopathic dilated cardiomyopathy.

Huang J, Xie CY, Kong XQ, Long MZ, Qiang MX, Ma WZ, Wang JL.

Chin Med J (Engl). 1994 Mar;107(3):176-80.

PMID:
7522141
12.

Familial automaticity-conduction disorder with associated cardiomyopathy.

Greenlee PR, Anderson JL, Lutz JR, Lindsay AE, Hagan AD.

West J Med. 1986 Jan;144(1):33-41.

13.

Report of the Committee on Methods of Linkage Analysis and Reporting.

Conneally PM, Edwards JH, Kidd KK, Lalouel JM, Morton NE, Ott J, White R.

Cytogenet Cell Genet. 1985;40(1-4):356-9. No abstract available.

PMID:
3864600
14.

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

Lathrop GM, Lalouel JM, Julier C, Ott J.

Am J Hum Genet. 1985 May;37(3):482-98.

15.

The EBV-hybridoma technique.

Roder JC, Cole SP, Kozbor D.

Methods Enzymol. 1986;121:140-67. No abstract available.

PMID:
3014265
16.
17.

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.

Orita M, Iwahana H, Kanazawa H, Hayashi K, Sekiya T.

Proc Natl Acad Sci U S A. 1989 Apr;86(8):2766-70.

18.

Prognostic features of children with idiopathic dilated cardiomyopathy.

Wiles HB, McArthur PD, Taylor AB, Gillette PC, Fyfe DA, Matthews JP, Shelton LW.

Am J Cardiol. 1991 Nov 15;68(13):1372-6.

PMID:
1835279
19.

Clinical characteristics of patients with dilated cardiomyopathy and bradyarrhythmias.

Ando S, Koyanagi S, Muramatsu K, Itaya R, Takeshita A, Nakamura M.

J Cardiol. 1991;21(1):53-9.

PMID:
1817181
20.

The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy.

Michels VV, Moll PP, Miller FA, Tajik AJ, Chu JS, Driscoll DJ, Burnett JC, Rodeheffer RJ, Chesebro JH, Tazelaar HD.

N Engl J Med. 1992 Jan 9;326(2):77-82.

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