-
1
-
-
0029784361
-
Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23
-
(1996)
J Clin Invest
, vol.98
, pp. 1355-1360
-
-
Bowles, K.R.1
Gajarski, R.2
Porter, P.3
Goytia, V.4
Bachinski, L.5
Roberts, R.6
Pignatelli, R.7
Towbin, J.A.8
-
3
-
-
8544283018
-
Penetrance of familial hypertrophic cardiomyopathy
-
(1997)
Genet Couns
, vol.8
, pp. 107-114
-
-
Charron, P.1
Carrier, L.2
Dubourg, O.3
Tesson, F.4
Desnos, M.5
Richard, P.6
Bonne, G.7
Guicheney, P.8
Hainque, B.9
Bouhour, J.B.10
Mallet, A.11
Feingold, J.12
Schwartz, K.13
Komajda, M.14
-
4
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5, 264 microsatellites
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenbach, J.14
-
5
-
-
0028801254
-
Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32
-
(1995)
Circulation
, vol.92
, pp. 3387-3389
-
-
Durand, J.B.1
Bachinski, L.L.2
Bieling, L.C.3
Czernuszewicz, G.Z.4
Abchee, A.B.5
Yu, Q.T.6
Tapscott, T.7
Hill, R.8
Ifegwu, J.9
Marian, A.J.10
Brugada, R.11
Daiger, S.12
Gregoritch, J.M.13
Anderson, J.L.14
Quinones, M.15
Towbin, J.A.16
Roberts, R.17
-
6
-
-
0033518282
-
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
-
(1999)
N Engl J Med
, vol.341
, pp. 1715-1724
-
-
Fatkin, D.1
MacRae, C.2
Sasaki, T.3
Wolff, M.R.4
Porcu, M.5
Frenneaux, M.6
Atherton, J.7
Vidaillet, H.J.8
Spudich, S.9
De Girolami, U.10
Seidman, J.G.11
Seidman, C.E.12
Muntoni, F.13
Muehle, G.14
Johnson, W.15
McDonough, B.16
-
9
-
-
0033358083
-
Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1068-1077
-
-
Jung, M.1
Poepping, I.2
Perrot, A.3
Ellmer, A.E.4
Wienker, T.F.5
Dietz, R.6
Reis, A.7
Osterziel, K.J.8
-
10
-
-
0028145745
-
A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1
-
(1994)
Nat Genet
, vol.7
, pp. 546-551
-
-
Kass, S.1
MacRae, C.2
Graber, H.L.3
Sparks, E.A.4
McNamara, D.5
Boudoulas, H.6
Basson, C.T.7
Baker III, P.B.8
Cody, R.J.9
Fishman, M.C.10
Cox, N.11
Kong, A.12
Wooley, C.F.13
Seidman, J.G.14
Seidman, C.E.15
-
11
-
-
0029009393
-
Familial dilated cardiomyopathy in the United Kingdom
-
(1995)
Br Heart J
, vol.73
, pp. 417-421
-
-
Keeling, P.J.1
Gang, Y.2
Smith, G.3
Seo, H.4
Bent, S.E.5
Murday, V.6
Caforio, A.L.7
McKenna, W.J.8
-
12
-
-
0029151478
-
Linkage of familial dilated cardiomyopathy to chromosome 9
-
Heart Muscle Disease Study Group
-
(1995)
Am J Hum Genet
, vol.57
, pp. 846-852
-
-
Krajinovic, M.1
Pinamonti, B.2
Sinagra, G.3
Vatta, M.4
Severini, G.M.5
Milasin, J.6
Falaschi, A.7
Giacca, M.8
-
13
-
-
0033520037
-
Desmin mutation responsible for idiopathic dilated cardiomyopathy
-
(1999)
Circulation
, vol.100
, pp. 461-464
-
-
Li, D.1
Tapscoft, T.2
Gonzalez, O.3
Butch, P.E.4
Quinones, M.A.5
Zoghbi, W.A.6
Hill, R.7
Bachinski, L.L.8
Mann, D.L.9
Roberts, R.10
-
14
-
-
0033494355
-
Familial dilated cardiomyopathy: Clinical features in French families
-
(1999)
Eur J Heart Failure
, vol.1
, pp. 353-361
-
-
Mangin, L.1
Charron, P.2
Tesson, F.3
Mallet, A.4
Dubourg, O.5
Desnos, M.6
Benaïche, A.7
Gayet, C.8
Gibelin, P.9
Davy, J.M.10
Bonnet, J.11
Sidi, D.12
Schwartz, K.13
Komajda, M.14
-
16
-
-
0032934453
-
Guidelines for the study of familial dilated cardiomyopathies
-
Collaborative Research Group of the European Human and Capital Mobility on Familial Dilated Cardiomyopathy
-
(1999)
Eur Heart J
, vol.20
, pp. 93-102
-
-
Mestroni, L.1
Maïsch, B.2
McKenna, W.J.3
Schwartz, K.4
Charron, P.5
Rocco, C.6
Tesson, F.7
Richter, A.8
Wilke, A.9
Komajda, M.10
-
17
-
-
0033165780
-
Familial dilated cardiomyopathy: Evidence for genetic and phenotypic heterogeneity
-
(1999)
J Am Coll Cardiol
, vol.34
, pp. 181-190
-
-
Mestroni, L.1
Rocco, C.2
Gregori, D.3
Sinagra, G.4
Di Lenarda, A.5
Miocic, S.6
Vatta, M.7
Pinamonti, B.8
Muntoni, F.9
Caforio, A.L.10
McKenna, W.J.11
Falaschi, A.12
Giacca, M.13
Camerini, F.14
-
18
-
-
0034724252
-
A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance
-
(2000)
Circulation
, vol.101
, pp. 1396-1402
-
-
Moolman, J.A.1
Reith, S.2
Uhl, K.3
Bailey, S.4
Gautel, M.5
Jeschke, B.6
Fischer, C.7
Ochs, J.8
McKenna, W.J.9
Klues, H.10
Vosberg, H.P.11
-
21
-
-
0343183359
-
Dilated cardiomyopathy and sensorineural hearing loss: A heritable syndrome that maps to 6q23-24
-
(2000)
Circulation
, vol.101
, pp. 1812-1818
-
-
Schönberger, J.1
Levy, H.2
Grünig, E.3
Sangwatanaroj, S.4
Fatkin, D.5
MacRae, C.6
Stäcker, H.7
Halpin, C.8
Eavey, R.9
Philbin, E.F.10
Katus, H.11
Seidman, J.G.12
Seidman, C.E.13
-
22
-
-
0033514986
-
Familial dilated cardiomyopathy locus maps to chromosome 2q31
-
(1999)
Circulation
, vol.99
, pp. 1022-1026
-
-
Siu, B.L.1
Niimura, H.2
Osborne, J.A.3
Fatkin, D.4
MacRae, C.5
Solomon, S.6
Benson, D.W.7
Seidman, J.G.8
Seidman, C.E.9
-
23
-
-
0033730389
-
Epidemiology of desmin and cardiac actin gene mutations in a European population of dilated cardiomyopathy
-
(2000)
Eur Heart J
, vol.21
, pp. 1872-1876
-
-
Tesson, F.1
Sylvius, N.2
Pilotto, A.3
Duboscq Bidot, L.4
Peuchmaurd, M.5
Bouchier, C.6
Bénaïche, A.7
Mangin, L.8
Charron, P.9
Gavazzi, A.10
Tavazzi, L.11
Arbustini, E.12
Komajda, M.13
-
24
-
-
0033818186
-
Mutations in the human δ-sarcoglycan gene in familial and sporadic dilated cardiomyopathy
-
(2000)
J Clin Invest
, vol.106
, pp. 655-662
-
-
Tsubata, S.1
Bowles, K.R.2
Vatta, M.3
Zintz, C.4
Titus, J.5
Muhonen, L.6
Bowles, N.E.7
Towbin, J.A.8
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