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Robustness of Massively Parallel Sequencing Platforms.
Kavak P, Yüksel B, Aksu S, Kulekci MO, Güngör T, Hach F, Şahinalp SC; Turkish Human Genome Project; Alkan C, Sağıroğlu MŞ. Kavak P, et al. Among authors: sagiroglu ms. PLoS One. 2015 Sep 18;10(9):e0138259. doi: 10.1371/journal.pone.0138259. eCollection 2015. PLoS One. 2015. PMID: 26382624 Free PMC article.
Whole-exome sequencing revealed two novel mutations in Usher syndrome.
Koparir A, Karatas OF, Atayoglu AT, Yuksel B, Sagiroglu MS, Seven M, Ulucan H, Yuksel A, Ozen M. Koparir A, et al. Among authors: sagiroglu ms. Gene. 2015 Jun 1;563(2):215-8. doi: 10.1016/j.gene.2015.03.060. Epub 2015 Mar 30. Gene. 2015. PMID: 25834954
Novel POC1A mutation in primordial dwarfism reveals new insights for centriole biogenesis.
Koparir A, Karatas OF, Yuceturk B, Yuksel B, Bayrak AO, Gerdan OF, Sagiroglu MS, Gezdirici A, Kirimtay K, Selcuk E, Karabay A, Creighton CJ, Yuksel A, Ozen M. Koparir A, et al. Among authors: sagiroglu ms. Hum Mol Genet. 2015 Oct 1;24(19):5378-87. doi: 10.1093/hmg/ddv261. Epub 2015 Jul 10. Hum Mol Genet. 2015. PMID: 26162852 Review.
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