Moleküler Biyoloji ve Genetik

Timur, A., Çağlayan, S.H., Aktuğlu, G., Gürgey, A., Ölek, K., “Point Mutations Identified in Turkish Hemophilia a Patients Using Denaturing Gradient Gel Electrophoresis (DGGE)”, Thrombosis and Haemostasis, PS926-PS926, 1997.

Türkçe

Çelik, A., Eraslan, S., Gökgöz, N., Ilgın, H., Başaran, S., Bokesoy, I., Kayserili, H., Apak, M.Y., Kırdar, B., “Identification of the Parental Origin of Polysomy in Two 49, XXXXY Cases”, Clinical Genetics, 51, 6, 426-429, 1997.

Türkçe

Eraslan, S., Gökgöz, N., Kırdar, B., “Identification of Deletion Carriers in Duchenne/Becker Muscular Dystrophy Families Using a Digoxigenin Labeled Quantitative Polymerase Chain Reaction Technique”, Molecular Diagnosis, 2, 4, 251-258, 1997.

Türkçe

Eraslan, S., Gökgöz, N., Kırdar, B., “Identification of Deletion Carriers in Duchenne/becker Muscular Dystrophy Families Using a Digoxigenin Labeled Quantitative Polymerase Chain Reaction Technique”, Molecular Diagnosis, 2, 4, 251-258, 1997.

Türkçe

Buğra, K., Hicks, D., “Acidic and Basic Fibroblast Growth Factor Messenger Rna and Protein Show Increased Expression in Adult Compared to Developing Normal and Dystrophic Rat Retina”, Journal of Molecular Neuroscience, 9, 1, 13-25, 1997.

Türkçe

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