Moleküler Biyoloji ve Genetik

Sıvacı, M., Parman, Y., Gonzaga-Jeuregui, C., Pehlivan, D., Durmuş, H., Deymeer, F., Oflazoğlu, P., Lupski, J.R., Battaloğlu, E., ' Exome sequencing vs phenotype directed gene screening in CMT patients from Turkey', Journal of Neurology,  Meeting Abstract: EP2163, 261, S146-S146, 2014.

Türkçe

Sıvacı, M., Parman, Y., Gonzaga-Jauregui, C., Pehlivan, D., Durmuş, H., Deymeer, F., Oflazoglu, P., Lupski, J.R., Battaloğlu, E.,'Exome sequencing vs. phenotype directed gene screening in CMT patients from Turkey', European Journal of Neurology,  Meeting Abstract: EP2163, 21, 209-209, 2014.

Türkçe

Özeş, B., Gonzalez, M., Durmuş, H., Deymeer, F., Oflazoğlu, P., Zuchner, S., Parman, Y., Battaloğlu, E., 'Whole exome sequencing analysis in recessive hereditary spastic paraplegia patients from Turkey', European Journal of Neurology,  Meeting Abstract: EP2162, 21, 209-209, 2014.

Türkçe

Özeş, B., Gonzalez, M., Durmuş, H., Deymeer, F Oflazoğlu, P., Zuchner, S., Parman, Y., Battaloğlu, E., 'Whole exome sequencing analysis in recessive hereditary spastic paraplegia patients from Turkey', Journal of Neurology,  Meeting Abstract: EP2162, 261, S145-S145, 2014.

Türkçe

Caballero Oteyza A, Battaloğlu E, Ocek L, Lindig T, Reichbauer J, Rebelo AP, Gonzalez MA, Zorlu Y, Ozes B, Timmann D, Bender B, Woehlke G, Züchner S, Schöls L, Schüle R, Motor protein mutations cause a new form of hereditary spastic paraplegia., Neurology, 82, 22, 2007-2016, 2014

Türkçe

Yıldırım, Y., Kerem, M., Köroğlu, C., Tolun, A., 'A homozygous 237-kb deletion at 1p31 identified as the locus for midline cleft of the upper and lower lip in a consanguineous family', European Journal of Human Genetics, 22, 3, 333-337, 2014.

Türkçe

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