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

av Hançer, Veysel Sabri, Gökgöz, Zafer, Büyükdoğan, Murat
I publikationen Turk J Haematol (2018)

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

av Hançer, Veysel Sabri, Fışgın, Tunç, Büyükdoğan, Murat
I publikationen Turk J Haematol (2020)

MPL W515L/K Mutations in Chronic Myeloproliferative Neoplasms

av Akpınar, Timur Selçuk, Hançer, Veysel Sabri, Nalçacı, Meliha, Diz-Küçükkaya, Reyhan
Publicerad 2013

Three Novel Calreticulin Mutations in Two Turkish Patients

av Hançer, Veysel Sabri, Tokgöz, Hüseyin, Güvenç, Serkan, Çalışkan, Ümran, Büyükdoğan, Murat
I publikationen Turk J Haematol (2017)

Prevalence of Human Papilloma Virus Types in Turkish and Albanian Women

av Hancer, Veysel Sabri, Buyukdogan, Murat, Bylykbashi, Ilta, Oksuz, Burcu, Acar, Muradiye
I publikationen J Cytol (2018)

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

av Alpay, Nilüfer, Hançer, Veysel Sabri, Erer, Burak, İnanç, Murat, Diz-Küçükkaya, Reyhan
I publikationen Turk J Haematol (2014)

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

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

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

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