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Veysel Sabri Hancer
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Journal Articles

Two Pediatric Cases of Essential Thrombocytopenia Characterized By Extremely Rare Mutations (CALR and MPL W515K)

Huseyin Tokgoz, Umran Caliskan, Reyhan Kucukkaya, Ahmet Demir, Veysel Sabri Hancer, PhD
Journal: Blood
Blood (2015) 126 (23): 4662.
https://doi.org/10.1182/blood.V126.23.4662.4662
Published: 2015
Journal Articles

Two Novel Mutations (p.I454T and p.Y472X) and a Homozygous p.A109T Mutation Associated with Factor XI Deficiency in a Turkish Family

Zafer Gokgoz, MD, Veysel Sabri Hancer, PhD, Reyhan Diz-Kucukkaya, MD
Journal: Blood
Blood (2014) 124 (21): 5054.
https://doi.org/10.1182/blood.V124.21.5054.5054
Published: 2014
Journal Articles

Can Activation Induced Cytidine Deaminase Lead to Genetic Instability in Bcr-Abl Negative Myeloproliferative Neoplasms?

Hasan Dermenci, Aynur Daglar, Basak Peker Akadam, Veysel Sabri Hancer, Yusuf Gelmez, Melih Aktan, Meliha Nalcaci, Akif S. Yavuz
Journal: Blood
Blood (2012) 120 (21): 5056.
https://doi.org/10.1182/blood.V120.21.5056.5056
Published: 2012
Journal Articles

Frequency and clinical outcomes of platelet membrane glycoprotein polymorphisms in antiphospholipid syndrome

Ipek Yonal, Fehmi Hindilerden, Veysel Sabri Hancer, Bahar Artim Esen, Meliha Nalcaci, Reyhan Diz Kucukkaya
Journal: Blood
Blood (2010) 116 (21): 3171.
https://doi.org/10.1182/blood.V116.21.3171.3171
Published: 2010
Journal Articles

Adamts-13 Gene Mutations and Transcription Analysis in Primary Antiphospholipid Syndrome.

Veysel sabri Hancer, Reyhan Diz-Kucukkaya, Aysegul topal-Sarikaya
Journal: Blood
Blood (2008) 112 (11): 1823.
https://doi.org/10.1182/blood.V112.11.1823.1823
Published: 2008
Journal Articles

CTLA-4 A49G Polymorphism and Autoimmune Blood Diseases.

Faruk Akturk, MD, Veysel Sabri Hancer, PhD, Serkan Guvenc, MD, Bahar Artim-esen, MD, Reyhan Diz-Kucukkaya, MD
Journal: Blood
Blood (2006) 108 (11): 3885.
https://doi.org/10.1182/blood.V108.11.3885.3885
Published: 2006