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Is cervical swab an efficient method for developing a new noninvasive prenatal diagnostic test for numerical and structural chromosome anomalies?
Yurtcu E, Karçaaltıncaba D, Kazan HH, Özdemir H, Yirmibeş Karaoğuz M, Çalış P, Kayhan G, Güntekin Ergün S, Perçin F, Bayram M, İlhan MN, Bilgili G, Kaymak T, Ergün MA. Yurtcu E, et al. Among authors: yirmibes karaoguz m. Turk J Med Sci. 2021 Jun 28;51(3):1043-1048. doi: 10.3906/sag-2009-347. Turk J Med Sci. 2021. PMID: 33315353 Free PMC article.
A case with a ring chromosome 22.
Koç A, Karaer K, Ergün MA, Yirmibeş-Karaoğuz M, Kan D, Cansu A, Perçin F. Koç A, et al. Among authors: yirmibes karaoguz m. Turk J Pediatr. 2008 Mar-Apr;50(2):193-6. Turk J Pediatr. 2008. PMID: 18664089
The importance of systematic genetic approach to familial schizophrenia cases and discussion of cryptic mosaic X chromosome aneuploidies in schizophrenia pathogenesis.
Koç A, Yirmibeş Karaoğuz M, Coşar B, Ferda Perçin E, Sahin S, Baysak E, Açikyürek K. Koç A, et al. Among authors: yirmibes karaoguz m. Int J Psychiatry Clin Pract. 2010 Sep;14(3):204-11. doi: 10.3109/13651501003802151. Epub 2010 Jul 20. Int J Psychiatry Clin Pract. 2010. PMID: 24917321