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Omics : a Journal of Integrative Biology|February 11, 2012
A molecular case report of autosomal dominant retinitis pigmentosa: RP1/RHO sequence variants in a Turkish familySinem M Nalbantoglu, Cahit Shahbazov, Afig Berdeli
Case Reports in Medicine|February 21, 2013
X-linked agammaglobulinemia presenting with secondary hemophagocytic syndrome: a case reportCan Ozturk, Sumer Sutcuoglu, Berna Atabay, et al.
Iranian Journal of Pediatrics|October 12, 2012
Association of FAS -670A/G and FASL -843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant PatientsPelin Ertan, Sevgi Mir, Nese Ozkayin, et al.
Turkish Journal of Medical Sciences|October 30, 2024
Distribution and classifications of <i>PKHD1</i> gene variants in a Turkish population using the next generation sequencing methodYüksel Gezgin, Berkay Kirnaz, Rauf Baylarov, et al.
The Turkish Journal of Gastroenterology : the Official Journal of Turkish Society of Gastroenterology|May 31, 2019
Distribution of nucleotide variants in the DNA sequence of ERCC1 and XRCC1 genes and the effect of phenotype in patients with gastric cancerElmir Asgerov, Özgür Şenol, Adem Güler, et al.
Archives of Oral Biology|June 22, 2006
Gingival crevicular fluid transforming growth factor-beta1 in several forms of periodontal diseaseAli Gürkan, Gülnur Emingil, Serhat Cinarcik, et al.
Archives of Oral Biology|January 8, 2011
A novel p.S34N mutation of CAMP gene in patients with periodontal diseaseOya Türkoğlu, Afig Berdeli, Gülnur Emingil, et al.
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