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    Chapter and Conference Paper

    Cytogenetic Studies in Familial Hypertrophic Cardiomyopathy: Identification of a Fragile Site on Human Chromosome 16

    A familial origin of hypertrophic cardiomyopathy was postulated from the first observations of the disease. In 1949 Evans described a syndrome having a distinct clinical, electrocardiographic, and pathological...

    M. Ambrosini, M. Ferraro, M. C. Maccaglia, R. Santoro in Advances in Cardiomyopathies (1990)