APA

Scheffold T., Kullmann S., Huge A., Binner P., Ochs H. R., Schöls W., Thale J., Motz W., Hegge F. J., Stellbrink C., Dorsel T., Gülker H., Heuer H., Dinh W., Stoll M. & Haltern G. (20120125). Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry. : BMC cardiovascular disorders.

Chicago

Scheffold Thomas, Kullmann Silke, Huge Andreas, Binner Priska, Ochs Hermann R, Schöls Wolfgang, Thale Joachim, Motz Wolfgang, Hegge Franz Josef, Stellbrink Christoph, Dorsel Thomas, Gülker Hartmut, Heuer Hubertus, Dinh Wilfried, Stoll Monika and Haltern Georg. 20120125. Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry. : BMC cardiovascular disorders.

Harvard

Scheffold T., Kullmann S., Huge A., Binner P., Ochs H. R., Schöls W., Thale J., Motz W., Hegge F. J., Stellbrink C., Dorsel T., Gülker H., Heuer H., Dinh W., Stoll M. and Haltern G. (20120125). Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry. : BMC cardiovascular disorders.

MLA

Scheffold Thomas, Kullmann Silke, Huge Andreas, Binner Priska, Ochs Hermann R, Schöls Wolfgang, Thale Joachim, Motz Wolfgang, Hegge Franz Josef, Stellbrink Christoph, Dorsel Thomas, Gülker Hartmut, Heuer Hubertus, Dinh Wilfried, Stoll Monika and Haltern Georg. Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry. : BMC cardiovascular disorders. 20120125.