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	1.	R506Q (FV Leiden) and R485K Mutations in the Factor V Gene: Incidence in Deep Venous Thrombosis and Hemophilia A Patients. [electronic resource] by Berber, Ergül Kavaklı, Kaan Akar, Nejat Berber, Eren Çağlayan, S Hande Producer: 20160829 In: Turkish journal of haematology : official journal of Turkish Society of Haematology vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	2.	Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p.M771I, p.L881R and p.P1413L. [electronic resource] by Berber, Ergul Ozbil, Mehmet Brown, Christine Baslar, Zafer Caglayan, S Hande Lillicrap, David Producer: 20180611 In: Blood transfusion = Trasfusione del sangue vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A common VWF exon 28 haplotype in the Turkish population. [electronic resource] by Berber, Ergul Pehlevan, Funda Akin, Mehmet Capan, Ozlem Yalcin Kavakli, Kaan Çaglayan, S Hande Producer: 20140617 In: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A novel missense mutation (N258S) in the KCNQ2 gene in a Turkish family afflicted with benign familial neonatal convulsions (BFNC). [electronic resource] by Yalçin, Ozlem Cağlayan, S Hande Saltik, Sema Cokar, Ozlem Ağan, Kadriye Dervent, Aysin Steinlein, Ortrud K Producer: 20080227 In: The Turkish journal of pediatrics vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	5.	Molecular pathology of haemophilia B in Turkish patients: identification of a large deletion and 33 independent point mutations. [electronic resource] by Onay, U Venüs Kavakli, Kaan Kilinç, Yurdanur Gürgey, Aytemiz Aktuğlu, Gülten Kemahli, Sabri Ozbek, Uğur Cağlayan, S Hande Producer: 20030429 In: British journal of haematology vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Factor 8 (F8) gene mutation profile of Turkish hemophilia A patients with inhibitors. [electronic resource] by Fidanci, Inanç D Kavakli, Kaan Uçar, Canan Timur, Cetin Meral, Adalet Kilinç, Yurdanur Sayilan, Hülya Kazanci, Elif Cağlayan, S Hande Producer: 20090818 In: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Association of a synonymous SCN1B variant affecting splicing efficiency with Benign Familial Infantile Epilepsy (BFIE). [electronic resource] by Usluer, Sunay Kayserili, Melek Aslı Eken, Aslı Gündoğdu Yiş, Uluc Leu, Costin Altmüller, Janine Thiele, Holger Nürnberg, Peter Sander, Thomas Çağlayan, S Hande Producer: 20180329 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations. [electronic resource] by Usluer, Sunay Salar, Seda Arslan, Mutluay Yiş, Uluç Kara, Bülent Tektürk, Pınar Baykan, Betül Meral, Cihan Türkdoğan, Dilşad Bebek, Nerses Yalçın Çapan, Özlem Gündoğdu Eken, Aslı Çağlayan, S Hande Producer: 20170213 In: Seizure vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)