Toplantı Özeti

Gökcümen, Ö., Alkan, C., Kavak, P., Somel, M., Uğurlu, S., Dal, E., Bugra-Bilge, K., Güngör, T., Şahinalp, C., Özören, N., Bekpen, C., 'Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and Africa', American Journal of Physical Anthropology, 153, 126-127, 2014.

Türkçe

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

Sayfalar