Characterization of the genetic basis of FXI deficiency in two Turkish patients by BERBER, E., RIMOLDI, V., USLUER, S., AKSU, S., PEKCELEN, Y., ÇAĞLAYAN, S. H., DUGA, S.

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Factor XIII Val34Leu polymorphism does not contribute to the prevention of thrombotic complications in patients with antiphospholipid syndrome by Diz-Kucukkaya, R, Hancer, V S, Inanc, M, Nalcaci, M, Pekcelen, Y

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The clinical and pharmacoeconomic analysis of invasive aspergillosis in adult patients with haematological diseases by Cagatay, A. Atahan, Cosan, F., Karadeniz, A., Besısık, S. K., Ozsut, H., Nalcaci, M., Pekcelen, Y., Eraksoy, H., Dincol, G., Calangu, S.

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Myeloid antigen expression provides favorable outcome in patients with adult acute lymphoblastic leukemia: a single-center study by YENEREL, M. N, ATAMER, T, DINCOL, G, YAVUZ, A. S, KUCUKKAYA, R, BESISIK, S, AKTAN, M, KESKIN, H, NALCACI, M, SARGIN, D, PEKCELEN, Y

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Conversion of an acute leukemia from a mixed lineage to lymphoid phenotype by Pekçelen, Yüksel, Timurağaoğlu, Ayşen

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P-selectin glycoprotein ligand-1 VNTR polymorphisms and risk of thrombosis in the antiphospholipid syndrome by Diz-Kucukkaya, Reyhan, Inanc, Murat, Afshar-Kharghan, Vahid, Zhang, Q Ed, López, José A, Pekcelen, Yuksel

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Possible etiologic factors in 151 Turkish patients with aplastic anemia by Alnıgeniş, M. Nergis, Nalçacı, Meliha, Pekçelen, Yüksel, Atamer, Tanju, Sargın, Deniz

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Bullous acral erythema and concomitant pigmentation on the face and occluded skin by Özkaya-Bayazit, Esen, Diz-Küçükkaya, Reyhan, Akasya, Esra, Büyükbabani, Nesimi, Öncü, Şeref, Pekçelen, Yüksel

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A different approach to telomere analysis with ddPRINS in chronic lymphocytic leukemia by Palanduz, Sukru, Serakinci, Nedime, Cefle, Kivanc, Aktan, Melih, Tutkan, Gulcin, Ozturk, Sukru, Bozkurt, Gokay, Dincol, Guncag, Pekcelen, Yuksel, Koch, Jørn

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Heparin And Ristocetin-Reduced Platelet Aggregation by Pekcelen, Y., Inceman, S.

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A Case of Chronic Lymphocytic Leukemia with a Constitutional Pericentric Inversion of Chromosome 1 by Palanduz, Şükrü, Çefle, Kivanç, Aktan, Melih, Tutkan, Gülçin, Öztürk, Şükrü, Pekçelen, Yüksel

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Characterization of the genetic basis of FXI deficiency in two Turkish patients by Berber, E, Rimoldi, V, Usluer, S, Aksu, S, Pekcelen, Y, Cağlayan, S H, Duga, S

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Letter: Heparin and ristocetin-reduced platelet aggregation by Pekcelen, Y, Inceman, S

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A different approach to telomere analysis with ddPRINS in chronic lymphocytic leukemia by PALANDUZ, S, SERAKINCI, N, CEFLE, K, AKTAN, M, TUTKAN, G, OZTURK, S, BOZKURT, G, DINCOL, G, PEKCELEN, Y, KOCH, J

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47,XYY Karyotype in Acute Myeloid Leukemia by Palanduz, Sukru, Aktan, Melih, Ozturk, Sukru, Tutkan, Gulcin, Cef le, Kivanc, Pekcelen, Yuksel

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Conversion of an acute leukemia from a mixed lineage to lymphoid phenotype by Pekçelen, Y, Timurağaoğlu, A

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