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

по Hançer, Veysel Sabri, Gökgöz, Zafer, Büyükdoğan, Murat
Опубликовано в: Turk J Haematol (2018)

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

по Hançer, Veysel Sabri, Fışgın, Tunç, Büyükdoğan, Murat
Опубликовано в: Turk J Haematol (2020)

MPL W515L/K Mutations in Chronic Myeloproliferative Neoplasms

по Akpınar, Timur Selçuk, Hançer, Veysel Sabri, Nalçacı, Meliha, Diz-Küçükkaya, Reyhan
Опубликовано 2013

Three Novel Calreticulin Mutations in Two Turkish Patients

по Hançer, Veysel Sabri, Tokgöz, Hüseyin, Güvenç, Serkan, Çalışkan, Ümran, Büyükdoğan, Murat
Опубликовано в: Turk J Haematol (2017)

Prevalence of Human Papilloma Virus Types in Turkish and Albanian Women

по Hancer, Veysel Sabri, Buyukdogan, Murat, Bylykbashi, Ilta, Oksuz, Burcu, Acar, Muradiye
Опубликовано в: J Cytol (2018)

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

по Alpay, Nilüfer, Hançer, Veysel Sabri, Erer, Burak, İnanç, Murat, Diz-Küçükkaya, Reyhan
Опубликовано в: Turk J Haematol (2014)

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

по Karacan, İlker, Diz Küçükkaya, Reyhan, Karakuş, Fatma Nur, Solakoğlu, Seyhun, Tolun, Aslıhan, Hançer, Veysel Sabri, Turanlı, Eda Tahir
Опубликовано в: Turk J Haematol (2019)

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

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