A large pedigree with valvuloseptal defects

American Journal of Cardiology

Volumn 80, Issue 7, 1997, Pages 968-970

  Schunkert, Heribert ^a,b   Bröckel, Ulrich ^a,b   Kromer, Eckhard P ^a,b   Elsner, Dietmar ^a,b   Jacob, Howard J ^a,b   Riegger, Günter A J ^a,b  

^a UNIVERSITY OF REGENSBURG   (Germany)

^b MEDICAL COLLEGE OF WISCONSIN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; FAMILY HISTORY; FEMALE; GENE CLUSTER; GENE LOCATION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; MALE; MOLECULAR GENETICS; PATHOGENESIS; PEDIGREE; PRIORITY JOURNAL; VALVULAR HEART DISEASE;

CHILD; CHILD, PRESCHOOL; FEMALE; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS; HUMANS; MALE; MUTATION; PEDIGREE;

EID: 0342602064     PISSN: 00029149     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9149(97)00560-2     Document Type: Article

References (5)

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2. Payne RM, Johnson MC, Grant JW, Strauss AW. Toward a molecular understanding of congenital heart disease. Circulation. 91:1995;494-504.
3. Nora JJ. Causes of congenital heart diseases: old and new modes, mechanisms, and models. Am Heart J. 125:1993;1409-1419.
4. Digilio MC, Marino B, Cicini MP, Giannotti A, Formigari R, Dallapiccola B. Risk of congenital heart defects in relatives of patients with atrioventricular canal. Am J Dis Child. 147:1993;1295-1297.
5. Whittemore R, Wells JA, Castellsague X. A second-generation study of 427 probands with congenital heart defects and their 837 children. J Am Coll Cardiol. 23:1994;1459-1467.