Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family

Autor Hançer, Veysel Sabri, Gökgöz, Zafer, Büyükdoğan, Murat
Vydáno v Turk J Haematol (2018)

Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia

Autor Hançer, Veysel Sabri, Fışgın, Tunç, Büyükdoğan, Murat
Vydáno v Turk J Haematol (2020)

MPL W515L/K Mutations in Chronic Myeloproliferative Neoplasms

Autor Akpınar, Timur Selçuk, Hançer, Veysel Sabri, Nalçacı, Meliha, Diz-Küçükkaya, Reyhan
Vydáno 2013

Three Novel Calreticulin Mutations in Two Turkish Patients

Autor Hançer, Veysel Sabri, Tokgöz, Hüseyin, Güvenç, Serkan, Çalışkan, Ümran, Büyükdoğan, Murat
Vydáno v Turk J Haematol (2017)

Prevalence of Human Papilloma Virus Types in Turkish and Albanian Women

Autor Hancer, Veysel Sabri, Buyukdogan, Murat, Bylykbashi, Ilta, Oksuz, Burcu, Acar, Muradiye
Vydáno v J Cytol (2018)

The Relationship between P-Selectin Polymorphisms and Thrombosis in Antiphospholipid Syndrome: A Pilot Case-Control Study

Autor Alpay, Nilüfer, Hançer, Veysel Sabri, Erer, Burak, İnanç, Murat, Diz-Küçükkaya, Reyhan
Vydáno v Turk J Haematol (2014)

A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing

Autor Karacan, İlker, Diz Küçükkaya, Reyhan, Karakuş, Fatma Nur, Solakoğlu, Seyhun, Tolun, Aslıhan, Hançer, Veysel Sabri, Turanlı, Eda Tahir
Vydáno v Turk J Haematol (2019)

Glycoprotein Ibα Kozak polymorphism in patients presenting with early-onset acute coronary syndrome

Autor Golcuk, Ebru, Yalin, Kivanc, Akdeniz, Cansu Selcan, Teker, Erhan, Teker, Başak, Hancer, Veysel Sabri, Altun, Ibrahim, Sezer, Murat, Kucukkaya, Reyhan Diz, Oncul, Aytac
Vydáno v Arch Med Sci (2016)