Echocardiographic features of genetic diseases: Part 1. Cardiomyopathy

Journal of the American Society of Echocardiography

Volumn 13, Issue 1, 2000, Pages 73-86

  Alizad, Azra ^a   Seward, James B ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BECKWITH WIEDEMANN SYNDROME; CARDIOMYOPATHY; CARNITINE DEFICIENCY; CLINICAL FEATURE; CONGENITAL HEART DISEASE; DIAGNOSTIC IMAGING; ECHOCARDIOGRAPHY; FAMILIAL DISEASE; FRIEDREICH ATAXIA; HEART DILATATION; HEART RIGHT VENTRICLE DYSPLASIA; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; LENTIGINOSIS; NOONAN SYNDROME; REVIEW;

EID: 0033956624     PISSN: 08947317     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0894-7317(00)90048-8     Document Type: Article

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