APA

Brøndum-Nielsen K., Beck B., Gyftodimou J., Hørlyk H., Liljenberg U., Petersen M. B., Pedersen W., Petersen M. B., Sand A., Skovby F., Stafanger G., Zetterqvist P. & Tommerup N. (19970220). Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms. : Human genetics.

Chicago

Brøndum-Nielsen K, Beck B, Gyftodimou J, Hørlyk H, Liljenberg U, Petersen M B, Pedersen W, Petersen M B, Sand A, Skovby F, Stafanger G, Zetterqvist P and Tommerup N. 19970220. Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms. : Human genetics.

Harvard

Brøndum-Nielsen K., Beck B., Gyftodimou J., Hørlyk H., Liljenberg U., Petersen M. B., Pedersen W., Petersen M. B., Sand A., Skovby F., Stafanger G., Zetterqvist P. and Tommerup N. (19970220). Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms. : Human genetics.

MLA

Brøndum-Nielsen K, Beck B, Gyftodimou J, Hørlyk H, Liljenberg U, Petersen M B, Pedersen W, Petersen M B, Sand A, Skovby F, Stafanger G, Zetterqvist P and Tommerup N. Investigation of deletions at 7q11.23 in 44 patients referred for Williams-Beuren syndrome, using FISH and four DNA polymorphisms. : Human genetics. 19970220.