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

di Hançer, Veysel Sabri, Gökgöz, Zafer, Büyükdoğan, Murat
Pubblicato in Turk J Haematol (2018)

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

di Hançer, Veysel Sabri, Fışgın, Tunç, Büyükdoğan, Murat
Pubblicato in Turk J Haematol (2020)

MPL W515L/K Mutations in Chronic Myeloproliferative Neoplasms

di Akpınar, Timur Selçuk, Hançer, Veysel Sabri, Nalçacı, Meliha, Diz-Küçükkaya, Reyhan
Pubblicazione 2013

Three Novel Calreticulin Mutations in Two Turkish Patients

di Hançer, Veysel Sabri, Tokgöz, Hüseyin, Güvenç, Serkan, Çalışkan, Ümran, Büyükdoğan, Murat
Pubblicato in Turk J Haematol (2017)

Prevalence of Human Papilloma Virus Types in Turkish and Albanian Women

di Hancer, Veysel Sabri, Buyukdogan, Murat, Bylykbashi, Ilta, Oksuz, Burcu, Acar, Muradiye
Pubblicato in J Cytol (2018)

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

di Alpay, Nilüfer, Hançer, Veysel Sabri, Erer, Burak, İnanç, Murat, Diz-Küçükkaya, Reyhan
Pubblicato in Turk J Haematol (2014)

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

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

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

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