The molecular basis of familial hypercholesterolaemia in Turkish patients von Sözen, M. Mert, Whittall, Ros, Öner, Cihan, Tokatlı, Ayşegül, Kalkanoğlu, H. Serap, Dursun, Ali, Coşkun, Turgay, Öner, Reyhan, Humphries, Steve E.

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Mutations in GNA11 in Uveal Melanoma von Van Raamsdonk, Catherine D, Griewank, Klaus G, Crosby, Michelle B, Garrido, Maria C, Vemula, Swapna, Wiesner, Thomas, Obenauf, Anna C, Wackernagel, Werner, Green, Gary, Bouvier, Nancy, Sozen, M. Mert, Baimukanova, Gail, Roy, Ritu, Heguy, Adriana, Dolgalev, Igor, Khanin, Raya, Busam, Klaus, Speicher, Michael R, O'Brien, Joan, Bastian, Boris C

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Three Novel Mutations in the Apolipoprotein E Gene in a Sample of Individuals with Type 2 Diabetes Mellitus von Stephens, Jeffrey W, Sozen, M. Mert, Whittall, Ros A, Caslake, Muriel J, Bedford, Dorothy, Acharya, Jayshree, Hurel, Steven J, Humphries, Steve E

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Genetic and molecular characterization of uveal melanoma cell lines von Griewank, K. G., Yu, X., Khalili, J., Sozen, M. M., Stempke-Hale, K., Bernatchez, C., Wardell, S., Bastian, B. C., Woodman, S. E.

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Complexed Prostate Specific Antigen Density is Better Than the Other PSA Derivatives for Detection of Prostate Cancer in Men with Total PSA between 2.5 and 20 ng/ml: Results of a P... von Sözen, Sinan, Eskicorapci, Saadettin, Küpeli, Bora, İrkilata, Lokman, Altinel, Mert, Özer, Gökhan, Uygur, Cemil, Alkibay, Turgut, Özen, Haluk

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Mutation detection in patients with familial hypercholesterolaemia using heteroduplex and single strand conformation polymorphism analysis by capillary electrophoresis von Sozen, Mert, Whittall, Roslyn, Humphries, Steve E.

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