Öner, A. F. Et Al. 2011. Recurrence of the p.Gly262Asp mutation and a novel p.Thr176_Gln186 deletion in twelve patients with congenital factor X deficiency. JOURNAL OF THROMBOSIS AND HAEMOSTASIS , vol.9 , 935-936.

Öner, A. F., Epcacan, S., Cairo, A., Menegatti, M., Akbayram, S., Peyvandi, F., ... Öner, A. F.(2011). Recurrence of the p.Gly262Asp mutation and a novel p.Thr176_Gln186 deletion in twelve patients with congenital factor X deficiency. JOURNAL OF THROMBOSIS AND HAEMOSTASIS , vol.9, 935-936.

Öner, Ahmet Et Al. "Recurrence of the p.Gly262Asp mutation and a novel p.Thr176_Gln186 deletion in twelve patients with congenital factor X deficiency," JOURNAL OF THROMBOSIS AND HAEMOSTASIS , vol.9, 935-936, 2011

Öner, Ahmet F. Et Al. "Recurrence of the p.Gly262Asp mutation and a novel p.Thr176_Gln186 deletion in twelve patients with congenital factor X deficiency." JOURNAL OF THROMBOSIS AND HAEMOSTASIS , vol.9, pp.935-936, 2011

Öner, A. F. Et Al. (2011) . "Recurrence of the p.Gly262Asp mutation and a novel p.Thr176_Gln186 deletion in twelve patients with congenital factor X deficiency." JOURNAL OF THROMBOSIS AND HAEMOSTASIS , vol.9, pp.935-936.

@article{article, author={Ahmet Fayik Öner Et Al. }, title={Recurrence of the p.Gly262Asp mutation and a novel p.Thr176_Gln186 deletion in twelve patients with congenital factor X deficiency}, journal={JOURNAL OF THROMBOSIS AND HAEMOSTASIS}, year=2011, pages={935-936} }