PROLONGED ATRIAL CONDUCTION/Leier, Meacham, Schaal

5. Anderson RC: Fetal and infant death, twinning and cardiac malformations in families of 2000 children with and without cardiac defects. Am J Cardiol 38: 218, 1976 6. Nora JJ, Nora AH: Genetics and Counseling in Cardiovascular Diseases. Springfield, Charles C Thomas, in press 7. Nora JJ, Nora AH, Sinha AK: The Ullrich-Noonan syndrome (Turner phenotype). Am J Dis Child 127: 48, 1974 8. Nora JJ, Lortscher RH, Spangler RD: Echocardiographic studies of left ventricular disease in Ullrich-Noonan syndrome. Am J Dis Child 129: 1417, 1975 9. Falconer DS: The inheritance of liability to certain diseases, estimated from the incidence among relatives. Ann Hum Genet 29: 51, 1965 10. Edwards JH: Familial predisposition in man. Br Med Bull 25: 58, 1969 11. Morton NE, Yee S, Elston RC, Lew R: Discontinuity and quasicontinuity: alternative hypotheses of multifactorial inheritance. Clin Genet 1: 81, 1970 12. Nora JJ, Sommerville RJ, Fraser FC: Homologies for congenital heart diseases: murine models influenced by dextroamphetamine. Teratology 1: 413, 1968 13. Wilson JG: Environment and Birth Defects. New York, Academic Press, 1973 14. Nora JJ, Nora AH, Toews WH: Lithium, Ebstein's anomaly and other congenital heart defects. Lancet 2: 594, 1974 15. Shapiro S, Hartz S, Siskind V, Mitchell A, Slone D, Rosenberg L, Monson R, Heinonen 0, Idanpaan-Heikkila J, Haro S, Saxen L: Anticonvulsants and parental epilepsy in the development of birth defects. Lancet 1: 273, 1976 16. Smith DW: Recognizable Patterns of Human Malformations, ed 2. Philadelphia, Saunders, 1976 17. Smith C: Recurrence risks for multifactorial inheritance. Am J Hum Genet 23: 578, 1971 18. Fuhrmann W: A family study in transposition of the great vessels and in tricuspid atresia. Humangenetik 6: 148, 1968 19. Fuhrmann W: Congenital heart disease in sibships ascertained by two affected siblings. Humangenetik 6: 1, 1968 20. Taussig HG, Crocetti A, Eshagh E: Follow-up of Blalock-Taussig operation. 1. Results of first operaion. Johns Hopkins Med J 129: 243, 1971 21. Sanchez-Cascos A: The recurrence risk in congenital heart disease. Presented to the 7th European Congress of Cardiology. Amsterdam, 1976 22. Chen S, Thompson MW, Rose V: Endocardial fibroelastosis: Family studies with special reference to counseling. J Pediatr 79: 385, 1971 23. Zoethout HE, Bonham-Carter RE, Carter CO: A family study of aortic stenosis. J Med Genet 1: 2, 1964 24. Jorgensen G, Beuren AJ: Genetische untersuchengen bei verschiedenen typen angeborener herz fehler. Monatschrift fur Kinderkeilkunde 119: 417, 1971 25. Williamson EM: A family study of atrial septal defect. J Med Genet 6: 255, 1969 26. Emanuel R, Nichols J, Anders JM, Moores EC, Somerville J: Atrioventricular defects a study of 92 families. Br Heart J 30: 645, 1968 27. Fraser FC, Hunter ADW: Etiologic relations among categories of congenital heart malformations. Am J Cardiol 36: 793, 1975 28. Rowland TW, Hubbel JP, Nadas AS: Congenital heart disease in infants of diabetic mothers. J Pediatr 83: 815, 1973 29. Holmes LB, Rose V, Child AH, Kratzer W: Comment on hypoplastic left heart syndrome. In Clinical Delineation of Birth Defects. XVI. Urinary System and Others. Baltimore, Williams and Wilkins, 1972, pp 228-230