Xq28-linked noncompaction of the left ventricular myocardium: Prenatal diagnosis and pathologic analysis of affected individuals

American Journal of Medical Genetics

Volumn 72, Issue 3, 1997, Pages 257-265

  Bleyl, Steven B ^a   Mumford, Brian R ^a   Brown Harrison, Mary Carole ^a   Pagotto, Luciana T ^a   Carey, John C ^a   Pysher, Theodore J ^a   Ward, Kenneth ^a   Chin, Thomas K ^a,b  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b East Tennessee State University   (United States)

Author keywords

Barth syndrome; Endocardial fibroelastosis; Isolated noncompaction of ventricular myocardium; Myotubular (centronuclear) myopathy; X linked cardiomyopathy

Indexed keywords

ARTICLE; CHROMOSOME XQ; CLINICAL ARTICLE; CONGENITAL HEART MALFORMATION; ECHOCARDIOGRAPHY; FAMILIAL DISEASE; FAMILY STUDY; FIBROELASTOSIS; GENETIC LINKAGE; HEART LEFT VENTRICLE FAILURE; HEART LEFT VENTRICLE FUNCTION; HEART VENTRICLE SEPTUM DEFECT; HEART VENTRICLE WALL; HISTOLOGY; HUMAN; INFANT; MITOCHONDRION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RECESSIVE INHERITANCE; X CHROMOSOME LINKAGE;

ADOLESCENT; CARDIOMYOPATHY, RESTRICTIVE; ECHOCARDIOGRAPHY; FEMALE; HEART VENTRICLES; HUMANS; INFANT; INFANT, NEWBORN; LINKAGE (GENETICS); MALE; MITOCHONDRIA, HEART; MYOCARDIUM; PEDIGREE; PRENATAL DIAGNOSIS; VENTRICULAR DYSFUNCTION, LEFT; X CHROMOSOME;

EID: 0030820393     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19971031)72:3<257::AID-AJMG2>3.0.CO;2-O     Document Type: Article

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