Çiftdoǧan, D. Y. Et Al. 2009. The Factor v G1691A, Factor v H1299R, prothrombin G20210A polymorphisms in children with family history of premature coronary artery disease. Coronary Artery Disease , vol.20, no.7 , 435-439.

Çiftdoǧan, D. Y., COŞKUN, Ş., ULMAN, C., & Tkz, H., (2009). The Factor v G1691A, Factor v H1299R, prothrombin G20210A polymorphisms in children with family history of premature coronary artery disease. Coronary Artery Disease , vol.20, no.7, 435-439.

Çiftdoǧan, Dilek Et Al. "The Factor v G1691A, Factor v H1299R, prothrombin G20210A polymorphisms in children with family history of premature coronary artery disease," Coronary Artery Disease , vol.20, no.7, 435-439, 2009

Çiftdoǧan, Dilek Y. Et Al. "The Factor v G1691A, Factor v H1299R, prothrombin G20210A polymorphisms in children with family history of premature coronary artery disease." Coronary Artery Disease , vol.20, no.7, pp.435-439, 2009

Çiftdoǧan, D. Y. Et Al. (2009) . "The Factor v G1691A, Factor v H1299R, prothrombin G20210A polymorphisms in children with family history of premature coronary artery disease." Coronary Artery Disease , vol.20, no.7, pp.435-439.

@article{article, author={Dilek Ylmaz Çiftdoǧan Et Al. }, title={The Factor v G1691A, Factor v H1299R, prothrombin G20210A polymorphisms in children with family history of premature coronary artery disease}, journal={Coronary Artery Disease}, year=2009, pages={435-439} }