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

Por Hançer, Veysel Sabri, Gökgöz, Zafer, Büyükdoğan, Murat
Publicado no Turk J Haematol (2018)

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

Por Hançer, Veysel Sabri, Fışgın, Tunç, Büyükdoğan, Murat
Publicado no Turk J Haematol (2020)

MPL W515L/K Mutations in Chronic Myeloproliferative Neoplasms

Por Akpınar, Timur Selçuk, Hançer, Veysel Sabri, Nalçacı, Meliha, Diz-Küçükkaya, Reyhan
Publicado em 2013

Three Novel Calreticulin Mutations in Two Turkish Patients

Por Hançer, Veysel Sabri, Tokgöz, Hüseyin, Güvenç, Serkan, Çalışkan, Ümran, Büyükdoğan, Murat
Publicado no Turk J Haematol (2017)

Prevalence of Human Papilloma Virus Types in Turkish and Albanian Women

Por Hancer, Veysel Sabri, Buyukdogan, Murat, Bylykbashi, Ilta, Oksuz, Burcu, Acar, Muradiye
Publicado no J Cytol (2018)

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

Por Alpay, Nilüfer, Hançer, Veysel Sabri, Erer, Burak, İnanç, Murat, Diz-Küçükkaya, Reyhan
Publicado no Turk J Haematol (2014)

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

Por Karacan, İlker, Diz Küçükkaya, Reyhan, Karakuş, Fatma Nur, Solakoğlu, Seyhun, Tolun, Aslıhan, Hançer, Veysel Sabri, Turanlı, Eda Tahir
Publicado no Turk J Haematol (2019)

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

Por Golcuk, Ebru, Yalin, Kivanc, Akdeniz, Cansu Selcan, Teker, Erhan, Teker, Başak, Hancer, Veysel Sabri, Altun, Ibrahim, Sezer, Murat, Kucukkaya, Reyhan Diz, Oncul, Aytac
Publicado no Arch Med Sci (2016)