-
1
-
-
0028886136
-
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
-
BONNE G., CARRIER L., BERCOVICI J., CRUAUD C., RICHARD P., HAINQUE B., GAUTEL M., LABEIT S., JAMES M., WEISSENBACH J., VOSBERG H.P., FISZMAN M., KOMAJDA M. and SCHWARTZ K. : Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nature genet., 1995, 11, 438-440.
-
(1995)
Nature Genet.
, vol.11
, pp. 438-440
-
-
Bonne, G.1
Carrier, L.2
Bercovici, J.3
Cruaud, C.4
Richard, P.5
Hainque, B.6
Gautel, M.7
Labeit, S.8
James, M.9
Weissenbach, J.10
Vosberg, H.P.11
Fiszman, M.12
Komajda, M.13
Schwartz, K.14
-
2
-
-
0023900843
-
Sex hormone modulation of ventricular hypertrophy in sinoaortic denervated rats
-
CABRAL A.M., VASQUEZ E.C., MOYSES M.R. and ANTONIO A.M. : Sex hormone modulation of ventricular hypertrophy in sinoaortic denervated rats. Hypertension, 1988, 11 (suppl I), I-93 - I-97.
-
(1988)
Hypertension
, vol.11
, Issue.1 SUPPL.
-
-
Cabral, A.M.1
Vasquez, E.C.2
Moyses, M.R.3
Antonio, A.M.4
-
3
-
-
0002131180
-
Distribution of disease loci in twenty eight french families with familial hypertrophic cardiomyopathy
-
abstract
-
CARRIER L., RICHARD P., BONNE G., BERCOVICI J., TESSON F., LAUTIE N., FORISSIER J.F., HAINQUE B., BENNACEUR M., GUICHENEY P., KOMAJDA M. and SCHWARTZ K. : Distribution of disease loci in twenty eight french families with familial hypertrophic cardiomyopathy. Circulation, 1995, 92, I-232 (abstract).
-
(1995)
Circulation
, vol.92
-
-
Carrier, L.1
Richard, P.2
Bonne, G.3
Bercovici, J.4
Tesson, F.5
Lautie, N.6
Forissier, J.F.7
Hainque, B.8
Bennaceur, M.9
Guicheney, P.10
Komajda, M.11
Schwartz, K.12
-
4
-
-
0027161005
-
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11
-
CARRIER L., HENGSTENBERG C., BECKMANN J.S., GUICHENEY P., DUFOUR C., BERCOVICI J., DAUSSE E., BEREBBI-BERTRAND I., WISNEWSKY C., PULVENIS D., FETLER L., VIGNAL A., WEISSENBACH J., HILLAIRE D., FEINGOLD J., BOUHOUR J.B., HAGEGE A., DESNOS M., ISNARD R., DUBOURG O., KOMAJDA M. and SCHWARTZ K. : Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11. Nature genet., 1993, 4, 311-314.
-
(1993)
Nature Genet.
, vol.4
, pp. 311-314
-
-
Carrier, L.1
Hengstenberg, C.2
Beckmann, J.S.3
Guicheney, P.4
Dufour, C.5
Bercovici, J.6
Dausse, E.7
Berebbi-Bertrand, I.8
Wisnewsky, C.9
Pulvenis, D.10
Fetler, L.11
Vignal, A.12
Weissenbach, J.13
Hillaire, D.14
Feingold, J.15
Bouhour, J.B.16
Hagege, A.17
Desnos, M.18
Isnard, R.19
Dubourg, O.20
Komajda, M.21
Schwartz, K.22
more..
-
5
-
-
0028818347
-
Hypertrophic cardiomyopathy in Tuscany : Clinical course and outcome in an unselected regional population
-
CECCHI .F, OLIVITTO I., MONTEREGGI A., SANTORO G., DOLARA A. and MARON B.J. : Hypertrophic cardiomyopathy in Tuscany : clinical course and outcome in an unselected regional population. J. Am. Col. Cardiol., 1995, 26, 1529-1536.
-
(1995)
J. Am. Col. Cardiol.
, vol.26
, pp. 1529-1536
-
-
Cecchi, F.1
Olivitto, I.2
Montereggi, A.3
Santoro, G.4
Dolara, A.5
Maron, B.J.6
-
6
-
-
0015914247
-
Familial Prevalence and Genetic Transmission of Idiopathic Subaortic Stenosis
-
CLARK C.E., HENRY W.L. and EPSTEIN S.E. : Familial Prevalence and Genetic Transmission of Idiopathic Subaortic Stenosis. N. Engl. J. Med., 1973, 289, 709-714.
-
(1973)
N. Engl. J. Med.
, vol.289
, pp. 709-714
-
-
Clark, C.E.1
Henry, W.L.2
Epstein, S.E.3
-
7
-
-
0027138216
-
Familial hypertrophic cardiomyopathy : Microsatellite haplotyping and identification of a hot spot for mutations in the β-myosin heavy chain gene
-
DAUSSE E., KOMAJDA M , FETLER L., DUBOURG O., DUFOUR C., CARRIER L., WINESNEWSKY C., BERCOVICI J., HENGSTENBERG C. AL-MAHDAWI S., ISNARD R., HAGEGE A., BOUHOUR J.B., DESNOS M., BECKMANN J.S., WEISSENBACH J., SCHWARTZ K. and GUICHENEY P. : Familial hypertrophic cardiomyopathy : microsatellite haplotyping and identification of a hot spot for mutations in the β-myosin heavy chain gene. J. Clin. Invest., 1993, 92, 2807-2813.
-
(1993)
J. Clin. Invest.
, vol.92
, pp. 2807-2813
-
-
Dausse, E.1
Komajda, M.2
Fetler, L.3
Dubourg, O.4
Dufour, C.5
Carrier, L.6
Winesnewsky, C.7
Bercovici, J.8
Hengstenberg, C.9
Al-Mahdawi, S.10
Isnard, R.11
Hagege, A.12
Bouhour, J.B.13
Desnos, M.14
Beckmann, J.S.15
Weissenbach, J.16
Schwartz, K.17
Guicheney, P.18
-
8
-
-
0028927133
-
Doppler echocardiography in familial hypertrophic cardiomyopathy : The french cooperative study
-
DUBOURG O., ISNARD R., HAGEGE A., JONDEAU G., DESNOS M., SACREZ A., BOUHOUR J.B., MESSMER PELLENC P., MILLAIRE A., FETLER L., GUICHENEY P., SCHWARTZ K. and KOMAJDA M. : Doppler echocardiography in familial hypertrophic cardiomyopathy : the french cooperative study. Echocardiography, 1995, 12, 235-40.
-
(1995)
Echocardiography
, vol.12
, pp. 235-240
-
-
Dubourg, O.1
Isnard, R.2
Hagege, A.3
Jondeau, G.4
Desnos, M.5
Sacrez, A.6
Bouhour, J.B.7
Messmer Pellenc, P.8
Millaire, A.9
Fetler, L.10
Guicheney, P.11
Schwartz, K.12
Komajda, M.13
-
9
-
-
0028145776
-
Identification of a mutation near a functionnal site of the β cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy
-
DUFOUR C., DAUSSE E., FETLER L., DUBOURG O., BOUHOUR J.B., VOSBERG H.-P., GUICHENEY., KOMAJDA M. and SCHWARTZ K. : Identification of a mutation near a functionnal site of the β cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol., 1994, 26, 1241-47.
-
(1994)
J. Mol. Cell. Cardiol.
, vol.26
, pp. 1241-1247
-
-
Dufour, C.1
Dausse, E.2
Fetler, L.3
Dubourg, O.4
Bouhour, J.B.5
Vosberg, H.-P.6
Guicheney7
Komajda, M.8
Schwartz, K.9
-
10
-
-
4243207053
-
Genomic organisation of human cardiac troponin Tgene : Relevance in mutation analysis in familial hypertrophic cardiomyopathy
-
abstract
-
FARZA H., TOWNSEND P.J., CARRIER L., FORISSIER J.F., KOMAJDA M., YACOUB M.H. and SCHWARTZ K. : Genomic organisation of human cardiac troponin Tgene : relevance in mutation analysis in familial hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol., 1996, 28, A35 (abstract).
-
(1996)
J. Mol. Cell. Cardiol.
, vol.28
-
-
Farza, H.1
Townsend, P.J.2
Carrier, L.3
Forissier, J.F.4
Komajda, M.5
Yacoub, M.H.6
Schwartz, K.7
-
11
-
-
0023127176
-
Effect of age, sex, body surface on echocardiographic left ventricular wall mass in normal subjects
-
GARDIN J.M., SAVAGE D.D., WARE J.H. and HENRY W.L. : Effect of age, sex, body surface on echocardiographic left ventricular wall mass in normal subjects. Hypertension, 1987, 9 (suppl. 2), II36-II39.
-
(1987)
Hypertension
, vol.9
, Issue.2 SUPPL.
-
-
Gardin, J.M.1
Savage, D.D.2
Ware, J.H.3
Henry, W.L.4
-
12
-
-
0025040392
-
A Molecular Basis for Familial Hypertrophic Cardiomyopathy : A β-Cardiac Myosin Heavy Chain Gene Missense Mutation
-
GEISTERFER-LOWRANCE A.A.T., KASS S., TANIGAWA G., VOSBERG H.-P., MCKENNA W., SEIDMAN C.E. and SEIDMAN J.G. : A Molecular Basis for Familial Hypertrophic Cardiomyopathy : a β-Cardiac Myosin Heavy Chain Gene Missense Mutation. Cell, 1990, 62, 999-1006.
-
(1990)
Cell
, vol.62
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.T.1
Kass, S.2
Tanigawa, G.3
Vosberg, H.-P.4
Mckenna, W.5
Seidman, C.E.6
Seidman, J.G.7
-
13
-
-
0030067394
-
A mouse model of Familial Hypertrophic Cardiomyopathy
-
GEISTERFER-LOWRANCE A.A.T., CHRISTE M., CONNER D.A., INGWALL J.S., SCHOEN F.J., SEIDMAN C.E. and SEIDMAN J.G. : A mouse model of Familial Hypertrophic Cardiomyopathy. Science, 1996, 272, 731-734.
-
(1996)
Science
, vol.272
, pp. 731-734
-
-
Geisterfer-Lowrance, A.A.T.1
Christe, M.2
Conner, D.A.3
Ingwall, J.S.4
Schoen, F.J.5
Seidman, C.E.6
Seidman, J.G.7
-
14
-
-
0023258399
-
Inheritance of hypertrophic cardiomyopathy : A cross sectional and M mode echocardiographic study of 50 families
-
GREAVES S.CV, ROCHE A.H.G., NEUTZE J.M., WHITLOCK R.M.L. and VEALE A.M.O. : Inheritance of hypertrophic cardiomyopathy : a cross sectional and M mode echocardiographic study of 50 families. Br. Heart. J., 1987, 58, 259-266.
-
(1987)
Br. Heart. J.
, vol.58
, pp. 259-266
-
-
Greaves, S.C.V.1
Roche, A.H.G.2
Neutze, J.M.3
Whitlock, R.M.L.4
Veale, A.M.O.5
-
15
-
-
0019165493
-
Echocardiographic measurements in normal subjects from infancy to old age
-
HENRY W.L., GARDIN J.M. and WARE J.H. : Echocardiographic measurements in normal subjects from infancy to old age. Circulation, 1980, 62, 1054-1066.
-
(1980)
Circulation
, vol.62
, pp. 1054-1066
-
-
Henry, W.L.1
Gardin, J.M.2
Ware, J.H.3
-
16
-
-
0024426784
-
Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1
-
JARCHO J.A., MC KENNA W., PETER PARE J.A., SOLOMON S.D., HOLCOMBE R.F., DICKIE S., LEVI T., DONIS-KELLER H., SEIDMAN J.G. and SEIDMAN C. : Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1. N. Engl. J. Med., 1989, 321, 1372-1378.
-
(1989)
N. Engl. J. Med.
, vol.321
, pp. 1372-1378
-
-
Jarcho, J.A.1
Mc Kenna, W.2
Peter Pare, J.A.3
Solomon, S.D.4
Holcombe, R.F.5
Dickie, S.6
Levi, T.7
Donis-Keller, H.8
Seidman, J.G.9
Seidman, C.10
-
17
-
-
0029143611
-
Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3
-
MACRAE C.A., GHAISAS N , KASS S., DONNELLY S., BASSON C.T., WATKINS H.C., ANAN R., THIERFELDER L.H., MCGARRY K., ROWLAND E., MCKENNA W.J., SEIDMAN J.G. and SEIDMAN C.E. : Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3. J. Clin. Invest., 1995, 96, 1216-20.
-
(1995)
J. Clin. Invest.
, vol.96
, pp. 1216-1220
-
-
Macrae, C.A.1
Ghaisas, N.2
Kass, S.3
Donnelly, S.4
Basson, C.T.5
Watkins, H.C.6
Anan, R.7
Thierfelder, L.H.8
Mcgarry, K.9
Rowland, E.10
Mckenna, W.J.11
Seidman, J.G.12
Seidman, C.E.13
-
18
-
-
0029083650
-
Prevalence of hypertrophic cardiomyopathy in a general population of young adults
-
MARON B.J., GARDIN J.M., FLACK J.M., GIDDING S.S., KUROSAKI T.T. and BILD D.E. : Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Circulation, 1995, 92, 785-89.
-
(1995)
Circulation
, vol.92
, pp. 785-789
-
-
Maron, B.J.1
Gardin, J.M.2
Flack, J.M.3
Gidding, S.S.4
Kurosaki, T.T.5
Bild, D.E.6
-
19
-
-
0023130164
-
Hypertrophic Cardiomyopathy : Interrelations of clinical manifestations, pathophysioiogy, and therapy
-
MARON B.J., BONOW R.O., CANNON R.O., LEON M.B. and EPSTEIN S E. Hypertrophic Cardiomyopathy : Interrelations of clinical manifestations, pathophysioiogy, and therapy. N. Engl. J. Med., 1987, 316, 780-789 / 844-852.
-
(1987)
N. Engl. J. Med.
, vol.316
, pp. 780-789
-
-
Maron, B.J.1
Bonow, R.O.2
Cannon, R.O.3
Leon, M.B.4
Epstein, S.E.5
-
20
-
-
0021346026
-
Patterns of inheritance in hypertrophic cardiomyopathy : Assessment by M-mode and two-dimensional echocardiography
-
MARON B.J , NICHOLS III P.F., PICKLE L.W., WESLEY Y.E. and MULVIHILL J.J. : Patterns of inheritance in hypertrophic cardiomyopathy : assessment by M-mode and two-dimensional echocardiography. Am. J. Cardiol.. 1984, 53, 1087-1094.
-
(1984)
Am. J. Cardiol..
, vol.53
, pp. 1087-1094
-
-
Maron, B.J.1
Nichols III, P.F.2
Pickle, L.W.3
Wesley, Y.E.4
Mulvihill, J.J.5
-
21
-
-
0022498091
-
Development and progression of left ventricular hypertrophy in children with hypertrophic cardiomyopathy
-
MARON B.J., SPIRITO P., WESLEY Y. and ARCE J. : Development and progression of left ventricular hypertrophy in children with hypertrophic cardiomyopathy. N. Engl. J. Med., 1986, 315, 610-14.
-
(1986)
N. Engl. J. Med.
, vol.315
, pp. 610-614
-
-
Maron, B.J.1
Spirito, P.2
Wesley, Y.3
Arce, J.4
-
22
-
-
15844400653
-
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle
-
POETTER K., JIANG H.E., HASSENZADEH S., MASTER S.R., CHANG A., DALAKAS M.C., RAYMENT I., SELLERS J.R., FANANAPAZIR L. and EPSTEIN N.D. : Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle. Nature genet., 1996, 13, 63-69.
-
(1996)
Nature Genet.
, vol.13
, pp. 63-69
-
-
Poetter, K.1
Jiang, H.E.2
Hassenzadeh, S.3
Master, S.R.4
Chang, A.5
Dalakas, M.C.6
Rayment, I.7
Sellers, J.R.8
Fananapazir, L.9
Epstein, N.D.10
-
23
-
-
0029864693
-
Report of the 1995 World Health Organisation / International Society and Federation of Cardiology task force on the definition and classification of cardiomyopathies
-
Report of the 1995 World Health Organisation / International Society and Federation of Cardiology task force on the definition and classification of cardiomyopathies. Circulation, 1996, 93, 841-842.
-
(1996)
Circulation
, vol.93
, pp. 841-842
-
-
-
24
-
-
0002707964
-
β-Myosin heavy chain gene mutations screening in 18 unrelated families with familial hypertrophic cardiomyopathy
-
abstract
-
RICHARD P., TESSON F., HAINQUE B., MATHIEU B., CARRIER L., KOMAJDA M., SCHWARTZ K. and GUICHENEY P. : β-Myosin heavy chain gene mutations screening in 18 unrelated families with familial hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol., 1996, 28, A65 (abstract).
-
(1996)
J. Mol. Cell. Cardiol.
, vol.28
-
-
Richard, P.1
Tesson, F.2
Hainque, B.3
Mathieu, B.4
Carrier, L.5
Komajda, M.6
Schwartz, K.7
Guicheney, P.8
-
25
-
-
0014300851
-
Point score system for the ECG diagnosis of left ventricular hypertrophy
-
ROMHILT D.W. and ESTES E.H. : Point score system for the ECG diagnosis of left ventricular hypertrophy. Am. Heart. J., 1968, 75, 752-758.
-
(1968)
Am. Heart. J.
, vol.75
, pp. 752-758
-
-
Romhilt, D.W.1
Estes, E.H.2
-
26
-
-
0025186513
-
Association of echocardiographic left ventricular mass with body size, blood pressure and physical activity
-
SAVAGE D.D., LEVY D., DANNENBERG A.L., GARRISON R.J. and CASTELLI W.P. : Association of echocardiographic left ventricular mass with body size, blood pressure and physical activity (the Framingham study). Am. J. Cardiol., 1990, 65, 371-376.
-
(1990)
Am. J. Cardiol.
, vol.65
, pp. 371-376
-
-
Savage, D.D.1
Levy, D.2
Dannenberg, A.L.3
Garrison, R.J.4
Castelli, W.P.5
-
27
-
-
0023189442
-
Effects of gonadectomy and hormonal replacement on rat hearts
-
SCHEUER J., MALHOTRA A., SHAIBLE T. .F. and CAPASSO J. : Effects of gonadectomy and hormonal replacement on rat hearts. Circ. Res., 1987, 61, 12-19.
-
(1987)
Circ. Res.
, vol.61
, pp. 12-19
-
-
Scheuer, J.1
Malhotra, A.2
Shaible, T.F.3
Capasso, J.4
-
28
-
-
0020561948
-
Distribution of left ventricular hypertrophy in hypertrophic cardiomyopathy : A two dimensional echocardiographic study
-
SHAPIRO L.M. and MCKENNA W.J. : Distribution of left ventricular hypertrophy in hypertrophic cardiomyopathy : a two dimensional echocardiographic study. J. Am. Coll. Cardiol., 1983, 2, 437-444.
-
(1983)
J. Am. Coll. Cardiol.
, vol.2
, pp. 437-444
-
-
Shapiro, L.M.1
Mckenna, W.J.2
-
29
-
-
0028840699
-
Gender differences in left ventricular growth
-
de SIMONE G., DEVEREUX R.B., DANIELS S.R. and MEYER R. A. : Gender differences in left ventricular growth. Hypertension, 1995, 26 (part 1), 979-983.
-
(1995)
Hypertension
, vol.26
, Issue.1 PART
, pp. 979-983
-
-
Simone, G.1
Devereux, R.B.2
Daniels, S.R.3
Meyer, R.A.4
-
30
-
-
0023245104
-
Absence of progression of left ventricular hypertrophy in adult patients with hypertrophic cardiomyopathy
-
SPIRITO P. and MARON B.J. : Absence of progression of left ventricular hypertrophy in adult patients with hypertrophic cardiomyopathy. J. Am. Coll. Cardiol., 1987, 9, 1013-1017.
-
(1987)
J. Am. Coll. Cardiol.
, vol.9
, pp. 1013-1017
-
-
Spirito, P.1
Maron, B.J.2
-
31
-
-
0028178083
-
α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy : A disease of the sarcomere
-
THIERFELDER L., WATKINS H., MACRAE C., LAMAS R., MCKENNA W., VOSBERG H.P., SEIDMAN J.G. and SEIDMAN C. : α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy : a disease of the sarcomere. Cell, 1994, 77, 701-712.
-
(1994)
Cell
, vol.77
, pp. 701-712
-
-
Thierfelder, L.1
Watkins, H.2
Macrae, C.3
Lamas, R.4
Mckenna, W.5
Vosberg, H.P.6
Seidman, J.G.7
Seidman, C.8
-
32
-
-
0027180678
-
A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2
-
THIERFELDER L., MACRAE C., WATKINS H., TOMFOHDE J., WILLIAMS M., MCKENNA W., BOHM K., NOESKE G., SCHLEPPER M., BOWCOCK A., VOSBERG H.-P., SEIDMAN J.G. and SEIDMAN C.E. : A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. Proc. Natl. Acad. Sci. USA, 1993, 90, 6270-6274.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 6270-6274
-
-
Thierfelder, L.1
Macrae, C.2
Watkins, H.3
Tomfohde, J.4
Williams, M.5
Mckenna, W.6
Bohm, K.7
Noeske, G.8
Schlepper, M.9
Bowcock, A.10
Vosberg, H.-P.11
Seidman, J.G.12
Seidman, C.E.13
-
33
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
WATKINS H., CONNER D., THIERFELDER L., JARCHO J.A., MACRAE C., MCKENNA W., MARON B.J., SEIDMAN J.G. and SEIDMAN C.E. : Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nature genet., 1995, 11, 434-437.
-
(1995)
Nature Genet.
, vol.11
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
Jarcho, J.A.4
Macrae, C.5
Mckenna, W.6
Maron, B.J.7
Seidman, J.G.8
Seidman, C.E.9
-
34
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy
-
WATKINS H., MCKENNA W., THIERFELDER L., SUK H.J., ANAN R., O'DONOGHUE A., SPIRITO P., MATSUMORI A., MORAVEC C.S., SEIDMAN J.G. and SEIDMAN C.E. : Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy. N. Engl. J. Med., 1995, 332, 1058-64.
-
(1995)
N. Engl. J. Med.
, vol.332
, pp. 1058-1064
-
-
Watkins, H.1
Mckenna, W.2
Thierfelder, L.3
Suk, H.J.4
Anan, R.5
O'Donoghue, A.6
Spirito, P.7
Matsumori, A.8
Moravec, C.S.9
Seidman, J.G.10
Seidman, C.E.11
-
35
-
-
0027420155
-
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3
-
WATKINS H., MACRAE C., THIERFELDER L., CHOU Y.-H., FRENNEAUX M., MCKENNA W., SEIDMAN J.G. and SEIDMAN C.E. : A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3. Nature genet., 1993, 3, 333-337.
-
(1993)
Nature Genet.
, vol.3
, pp. 333-337
-
-
Watkins, H.1
Macrae, C.2
Thierfelder, L.3
Chou, Y.-H.4
Frenneaux, M.5
Mckenna, W.6
Seidman, J.G.7
Seidman, C.E.8
|