Items where Author is "Cengiz, F.B."

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Bademci, G. and Foster, II and Mahdieh, N. and Bonyadi, M. and Duman, D. and Cengiz, F.B. and Menendez, I. and Diaz-Horta, O. and Shirkavand, A. and Zeinali, S. and Subasioglu, A. and Tokgoz-Yilmaz, S. and Huesca-Hernandez, F. and De La Luz Arenas-Sordo, M. and Dominguez-Aburto, J. and Hernandez-Zamora, E. and Montenegro, P. and Paredes, R. and Moreta, G. and Vinueza, R. and Villegas, F. and Mendoza-Benitez, S. and Guo, S. and Bozan, N. and Tos, T. and Incesulu, A. and Sennaroglu, G. and Blanton, S.H. and Ozturkmen-Akay, H. and Yildirim-Baylan, M. and Tekin, M. (2016) Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. Genetics in Medicine, 18 (4). pp. 364-371.

Bademci, G. and Cengiz, F.B. and Foster, II and Duman, D. and Sennaroglu, L. and Diaz-Horta, O. and Atik, T. and Kirazli, T. and Olgun, L. and Alper, H. and Menendez, I. and Loclar, I. and Sennaroglu, G. and Tokgoz-Yilmaz, S. and Guo, S. and Olgun, Y. and Mahdieh, N. and Bonyadi, M. and Bozan, N. and Ayral, A. and Ozkinay, F. and Yildirim-Baylan, M. and Blanton, S.H. and Tekin, M. (2016) Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss. Scientific Reports, 6.

This list was generated on Fri Jan 17 16:39:35 2020 +0330.