Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia von Hançer, Veysel Sabri, Fışgın, Tunç, Büyükdoğan, Murat

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Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family von Hançer, Veysel Sabri, Gökgöz, Zafer, Büyükdoğan, Murat

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Three Novel Calreticulin Mutations in Two Turkish Patients von Hançer, Veysel Sabri, Tokgöz, Hüseyin, Güvenç, Serkan, Çalışkan, Ümran, Büyükdoğan, Murat

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The Relationship between P-Selectin Polymorphisms and Thrombosis in Antiphospholipid Syndrome: A Pilot Case-Control Study von Alpay, Nilüfer, Hançer, Veysel Sabri, Erer, Burak, İnanç, Murat, Diz-Küçükkaya, Reyhan

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MPL W515L/K Mutations in Chronic Myeloproliferative Neoplasms von Akpınar, Timur Selçuk, Hançer, Veysel Sabri, Nalçacı, Meliha, Diz-Küçükkaya, Reyhan

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A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing von Karacan, İlker, Diz Küçükkaya, Reyhan, Karakuş, Fatma Nur, Solakoğlu, Seyhun, Tolun, Aslıhan, Hançer, Veysel Sabri, Turanlı, Eda Tahir

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ADAMTS-13 gene expression in antiphospholipid syndrome von Hancer, Veysel Sabri, Diz Kucukkaya, Reyhan, Topal Sarikaya, Aysegul

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Cytotoxic T lymphocyte antigen-4 (CTLA-4) A49G polymorphism and autoimmune blood diseases von Akturk, Faruk, Hancer, Veysel Sabri, Kuçukkaya, Reyhan

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INVESTIGATION OF PTGS2, MAGE-A3, CALR, KRT19 AND TMPRSS4 EXPRESSIONS IN HCT116 COLON CANCER AND PC3 PROSTATE CANCER CELL LINES von Bozkurt, Süreyya, Yarımcan, Filiz, Ayhan, Hüseyin, Kotan, Hacer, Tuğçe Sezgin, Hüma, Çınar, Elif, Aynacı, Ceren, Okan Akar, Remzi, Hançer, Veysel Sabri

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Coronary Artery Ectasia Is Associated with the c.894G>T (Glu298Asp) Polymorphism of the Endothelial Nitric Oxide Synthase Gene von Yalcin, Ahmet Arif, Akturk, Ibrahim Faruk, Celik, Omer, Erturk, Mehmet, Hancer, Veysel Sabri, Yalcin, Burce, Isiksacan, Nilgun, Uzun, Fatih, Ozyilmaz, Sinem Ozbey, Biyik, Ismail

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Novel RUNX1 Variation in B-cell Acute Lymphoblastic Leukemia von Qipa, Egzona, Acar, Muradiye, Bozkurt, Sureyya, Buyukdogan, Murat, Sonmez, Hazal B, Sayitoglu, Muge, Erbilgin, Yucel, Karakaş, Zeynep, Hançer, Veysel S

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New indicator of cellular ischemia in coronary slow-flow phenomenon: Cell-free DNA von Yolcu, Mustafa, Dogan, Ali, Kurtoglu, Nuri, Hancer, Veysel Sabri, Gürbüzel, Mehmet

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Beta 2 glycoprotein I Valine247Leucine polymorphism in patients with antiphospholipid syndrome von Tekeoglu, Senem, Hancer, Veysel Sabri, Artim-Esen, Bahar, Nalcaci, Meliha, Inanc, Murat

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The relationship between clinical parameters and hepatocyte growth factor/c-Met levels in the sperm of infertile males

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Prevalence of human papilloma virus types in Turkish and Albanian women von Hancer, Veysel, Buyukdogan, Murat, Bylykbashi, Ilta, Oksuz, Burcu, Acar, Muradiye

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The Association Between Factor XIII Val34Leu Polymorphism and Early Myocardial Infarction von Hancer, Veysel Sabri, Diz-Kucukkaya, Reyhan, Bilge, Ahmet Kaya, Ozben, Beste, Oncul, Aytac, Ergen, Gursel, Nalcaci, Meliha

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ADAMTS-13 gene expression in antiphospholipid syndrome / Antifosfolipid sendromunda ADAMTS-13 gen ekspresyonu von Hancer, Veysel Sabri, Kucukkaya, Reyhan Diz, Topal-Sarikaya, Aysegul

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Aberrant Activation-Induced Cytidine Deaminase Gene Expression Links BCR/ABL1-Negative Classical Myeloproliferative Neoplasms von Dermenci, Hasan, Daglar Aday, Aynur, Akadam Teker, Aysegul Basak, Hancer, Veysel Sabri, Gelmez, Metin Yusuf, Nalcaci, Meliha, Yavuz, Akif Selim

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The impact of platelet membrane glycoprotein Ib alpha and Ia/IIa polymorphisms on the risk of thrombosis in the antiphospholipid syndrome von Yonal, Ipek, Hindilerden, Fehmi, Hancer, Veysel Sabri, Artim-Esen, Bahar, Daglar, Aynur, Akadam, Basak, Nalcaci, Meliha, Diz-Kucukkaya, Reyhan

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Glycoprotein Ibα Kozak polymorphism in patients presenting with early-onset acute coronary syndrome von Golcuk, Ebru, Yalin, Kivanc, Akdeniz, Cansu Selcan, Teker, Erhan, Teker, Başak, Hancer, Veysel Sabri, Altun, Ibrahim, Sezer, Murat, Kucukkaya, Reyhan Diz, Oncul, Aytac

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