Search Results - TAPSCOTT, Terry

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  1. 1
    Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23

    Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23 by AHMAD, F, DUANXIANG LI, BACHINSKI, L. L, ROBERTS, R, KARIBE, A, GONZALEZ, O, TAPSCOTT, T, HILL, R, WEILBAECHER, D, BLACKIE, P, FUREY, M, GARDNER, M

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  2. 2
    The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14

    The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14 by Li, Duanxiang, Ahmad, Ferhaan, Gardner, Martin J., Weilbaecher, Donald, Hill, Rita, Karibe, Akihiko, Gonzalez, Oscar, Tapscott, Terry, Sharratt, Geoffrey P., Bachinski, Linda L., Roberts, Robert

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  3. 3
    Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32

    Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32 by DURAND, J.-B, BACHINSKI, L. L, BRUGADA, R, DAIGER, S, GREGORITCH, J. M, ANDERSON, J. L, QUINONES, M, TOWBIN, J. A, ROBERTS, R, BIELING, L. C, CZERNUSZEWICZ, G. Z, ABCHEE, A. B, QUN TAO YU, TAPSCOTT, T, HILL, R, IFEGWU, J, MARIAN, A. J

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  4. 4
    Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy

    Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy by GOLLOB, Michael H, SEGER, John J, GOLLOB, Tanya N, TAPSCOTT, Terry, GONZALES, Oscar, BACHINSKI, Linda, ROBERTS, Robert

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  5. 5
    Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

    Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy by DUANXIANG LI, CZERNUSZEWICZ, Grazyna Z, QUINONES, Miguel, BACHINSKI, Linda L, ROBERTS, Robert, GONZALEZ, Oscar, TAPSCOTT, Terry, KARIBE, Akihiko, DURAND, Jean-Bernard, BRUGADA, Ramon, HILL, Rita, GREGORITCH, Jane M, ANDERSON, Jeffrey L

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  6. 6
    Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population

    Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population by HEJTMANCIK, J. F, BRINK, P. A, TOWBIN, J, HILL, R, BRINK, L, TAPSCOTT, T, TRAKHTENBROIT, A, ROBERTS, R

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  7. 7
    Localization of the gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse American population

    Localization of the gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse American population by Hejtmancik, J.Fielding, Brink, Paul A., Towbin, Jeffrey, Hill, Rita, Brink, Lucy, Czemuszewicz, Grazyna Z, Tapscott, Terry, Trakhtenbrolt, Anatole, Perryman, M.Benjamin, Roberts, Robert

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