Causes of congenital heart diseases: old and new modes, mechanisms, and models.

[1]  D. Wallace,et al.  Heart disease and mitochondrial DNA mutations. , 1992, Heart disease and stroke : a journal for primary care physicians.

[2]  J. Hall Genomic imprinting and its clinical implications. , 1992, The New England journal of medicine.

[3]  H. Smeets,et al.  Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15. , 1992, The New England journal of medicine.

[4]  K. Berg,et al.  Cardiovascular Diseases: Genetics, Epidemiology and Prevention , 1991 .

[5]  E. Clark,et al.  Developmental Cardiology: Morphogenesis and Function , 1990 .

[6]  J. Hall,et al.  Genomic imprinting: review and relevance to human diseases. , 1990, American journal of human genetics.

[7]  J. Knoll,et al.  Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome , 1989, Nature.

[8]  E. Murphy,et al.  Genetics and congenital heart disease: perspectives and prospects. , 1989, Journal of the American College of Cardiology.

[9]  Sangkot Marzuki,et al.  MITOCHONDRIAL DNA MUTATIONS AS AN IMPORTANT CONTRIBUTOR TO AGEING AND DEGENERATIVE DISEASES , 1989, The Lancet.

[10]  J. Edwards Familiarity, recessivity and germline mosaicism , 1989, Annals of human genetics.

[11]  G. Ponsot,et al.  KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION , 1988, The Lancet.

[12]  D. Ledbetter,et al.  Uniparental disomy as a mechanism for human genetic disease. , 1988, American journal of human genetics.

[13]  J. Nora,et al.  Maternal transmission of congenital heart diseases: new recurrence risk figures and the questions of cytoplasmic inheritance and vulnerability to teratogens. , 1987, The American journal of cardiology.

[14]  F. Sanger,et al.  Sequence and organization of the human mitochondrial genome , 1981, Nature.

[15]  J I Hoffman,et al.  Congenital heart disease in a cohort of 19,502 births with long-term follow-up. , 1978, The American journal of cardiology.

[16]  J. Nora,et al.  The Evolution of Specific Genetic and Environmental Counseling in Congenital Heart Diseases , 1978, Circulation.

[17]  F. Fraser,et al.  Etiologic relations among categories of congenital heart malformations. , 1975, The American journal of cardiology.

[18]  D. Patterson,et al.  Hereditary defects of the conotruncal septum in Keeshond dogs: pathologic and genetic studies. , 1974, The American journal of cardiology.

[19]  M. Nihill,et al.  Antiheart antibody production of cardiovascular malformations in the mouse: a preliminary study. , 1974, Teratology.

[20]  C. Smith Recurrence risks for multifactorial inheritance. , 1971, American journal of human genetics.

[21]  F. Fraser,et al.  Homologies for congenital heart diseases: murine models, influenced by dextroamphetamine. , 1968, Teratology.

[22]  J. Nora,et al.  Multifactorial Inheritance Hypothesis for the Etiology of Congenital Heart Diseases: The Genetic‐Environmental Interaction , 1968, Circulation.

[23]  C. P. Dagg Combined action of fluorouracil and two mutant genes on limb development in the mouse. , 1967, The Journal of experimental zoology.

[24]  T. Ozawa,et al.  Hypothesis. Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases , 1989 .

[25]  J. Nora,et al.  Congenital heart disease : causes and processes , 1984 .

[26]  Nora Jj,et al.  Genetic epidemiology of congenital heart diseases. , 1983 .