Fen-Edebiyat Fakültesi

Yıldırım, Y., Orhan, E.K., İşeri, S.A.U., Serdaroglu-Oflazer, P., Kara, B., Solakoğlu, S., Tolun, A., “A frameshift mutation of ERLIN2 in recessive intellectual disability, motor dysfunction and multiple joint contractures”, Human Molecular Genetics, 20, 10, 1886-1892, 2011.

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Yıldırım, Y., Tolun, A., Tüysüz, B., “The phenotype caused by pycr1 mutations corresponds to geroderma osteodysplasticum rather than autosomal recessive cutis laxa type 2”, American Journal of Medical Genetics Part A, 155A, 1, 134-140, 2011.

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Sin, B.A., Akdiş, M., Zumkehr, J., Bezzine, S., Bekpen, C., Lambeau, G., Akdiş, C.A., “T-cell and antibody responses to phospholipase A(2) from different species show distinct cross reactivity patterns”, Allergy, 66, 12, 1513-1521, 2011.

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