APA

Goddard K. A., Yu C. E., Oshima J., Miki T., Nakura J., Piussan C., Martin G. M., Schellenberg G. D. & Wijsman E. M. (19960725). Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers. : American journal of human genetics.

Chicago

Goddard K A, Yu C E, Oshima J, Miki T, Nakura J, Piussan C, Martin G M, Schellenberg G D and Wijsman E M. 19960725. Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers. : American journal of human genetics.

Harvard

Goddard K. A., Yu C. E., Oshima J., Miki T., Nakura J., Piussan C., Martin G. M., Schellenberg G. D. and Wijsman E. M. (19960725). Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers. : American journal of human genetics.

MLA

Goddard K A, Yu C E, Oshima J, Miki T, Nakura J, Piussan C, Martin G M, Schellenberg G D and Wijsman E M. Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers. : American journal of human genetics. 19960725.