S. A. Ugur And A. Tolun, "A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.2, pp.261-264, 2008
Ugur, S. A. And Tolun, A. 2008. A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.2 , 261-264.
Ugur, S. A., & Tolun, A., (2008). A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.2, 261-264.
Ugur, Sibel, And Aslihan Tolun. "A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.2, 261-264, 2008
Ugur, Sibel A. And Tolun, Aslihan. "A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.2, pp.261-264, 2008
Ugur, S. A. And Tolun, A. (2008) . "A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.16, no.2, pp.261-264.
@article{article, author={Sibel Aylin UĞUR İŞERİ And author={Aslihan Tolun}, title={A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2008, pages={261-264} }