APA

Ferda Percin E., Ploder L. A., Yu J. J., Arici K., Horsford D. J., Rutherford A., Bapat B., Cox D. W., Duncan A. M., Kalnins V. I., Kocak-Altintas A., Sowden J. C., Traboulsi E., Sarfarazi M. & McInnes R. R. (20000828). Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. : Nature genetics.

Chicago

Ferda Percin E, Ploder L A, Yu J J, Arici K, Horsford D J, Rutherford A, Bapat B, Cox D W, Duncan A M, Kalnins V I, Kocak-Altintas A, Sowden J C, Traboulsi E, Sarfarazi M and McInnes R R. 20000828. Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. : Nature genetics.

Harvard

Ferda Percin E., Ploder L. A., Yu J. J., Arici K., Horsford D. J., Rutherford A., Bapat B., Cox D. W., Duncan A. M., Kalnins V. I., Kocak-Altintas A., Sowden J. C., Traboulsi E., Sarfarazi M. and McInnes R. R. (20000828). Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. : Nature genetics.

MLA

Ferda Percin E, Ploder L A, Yu J J, Arici K, Horsford D J, Rutherford A, Bapat B, Cox D W, Duncan A M, Kalnins V I, Kocak-Altintas A, Sowden J C, Traboulsi E, Sarfarazi M and McInnes R R. Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. : Nature genetics. 20000828.