H. Graber

发表

Calcification of the mitral annulus: etiology, clinical associations, complications and therapy.

B. M. Beaver, P. K. Fulkerson, J. Auseon, 1979, The American journal of medicine.

Evolution of a hereditary cardiac conduction and muscle disorder: a study involving a family with six generations affected.

J. Ryan, P. Baker, C. Wooley, 1986, Circulation.

Heritable Cardiac Conduction and Myocardial Disease: From the Clinic to the Basic Science Laboratory and Back to the Clinic

C. Seidman, S. Raman, H. Boudoulas, 2011, Cardiology.

Clinical characteristics of sudden death victims in heritable (chromosome 1p1-1q1) conduction and myocardial disease.

P. Baker, C. Wooley, H. Boudoulas, 1998, Journal of the American College of Cardiology.

Anti-beta-receptor antibodies in familial cardiomyopathy: correlation with HLA-DR and HLA-DQ gene polymorphisms.

C. Wooley, H. Boudoulas, C. Limas, 1994, American heart journal.

Genetic aspects of idiopathic epilepsy in Labrador retrievers.

A. Jaggy, C. Gaillard, H. Graber, 1998, The Journal of small animal practice.

T-cell receptor gene polymorphisms in familial cardiomyopathy: Correlation with anti-β-receptor autoantibodies

C. Wooley, H. Boudoulas, C. Limas, 1992 .

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1

A. Kong, J. Seidman, M. Fishman, 1994, Nature Genetics.

Atrial myopathy and atrial fibrillation : phenotypes in heritable cardiac conduction and myocardial disease

C. Wooley, H. Boudoulas, S. Nelson, 2000 .

HLA-DQA1 and -DQB1 gene haplotypes in familial cardiomyopathy.

C. Wooley, H. Boudoulas, C. Limas, 1994, The American journal of cardiology.