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American Journal of Medical Genetics. Part A|January 31, 2014
Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversionAyse Gul Zamani, Aynur Acar, Gul Durakbasi-Dursun, et al.Medicine International|June 28, 2024
Dynein axonemal heavy chain 9 M4374I variation may have an effect on imatinib mesylate resistance in CMLMahmut Selman Yildirim, Levent Şi Mşek, Ayşe Gül Zamani, et al.Cancer Genetics and Cytogenetics|August 30, 2006
Relation of glutathione S-transferase genotypes (GSTM1 and GSTT1) to laryngeal squamous cell carcinoma riskHasan Acar, Kayhan Ozturk, M Hamza Muslumanoglu, et al.Journal of Gastrointestinal Cancer|May 16, 2023
The Effect of RAS/BRAF Mutation Status on Prognosis and Relapse Pattern in Early Stage Colon CancersNazli Kunt, Murat Araz, Mahmut Selman Yildirim, et al.Journal of Pediatric Ophthalmology and Strabismus|May 17, 2016
Ocular Findings in Children With 22q11.2 Deletion SyndromeBahar Gokturk, Pinar Topcu-Yilmaz, Banu Bozkurt, et al.Asian Pacific Journal of Allergy and Immunology|March 24, 2016
Would mean platelet volume/platelet count ratio be used as a novel formula to predict 22q11.2 deletion syndrome?Bahar Gokturk, Sukru Nail Guner, Reyhan Kara, et al.Psychiatry Research|May 15, 2026
Psychotic vulnerability in pediatric OCD: associations with neurocognitive functioningOmca Guney, Abdullah Yaser Guney, Selman Yildirim, et al.Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|January 19, 2015
Prognostic value of ERCC1, ERCC2, XRCC1, and TP53 single nucleotide polymorphisms in patients with early-stage non-small cell lung cancerCaglayan Geredeli, Mehmet Artac, Selman Yildirim, et al.Journal of Clinical Immunology|March 26, 2026
A Novel Pathogenic Variant in TRAC Gene Associated with SCID Phenotype: Expanding the Genetic and Clinical SpectrumMehmet Ali Karaselek, Mehmet Yavuz Ozbey, Vedat Uygun, et al.American Journal of Medical Genetics. Part A|July 22, 2014
Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndromeYavuz Bayram, Davut Pehlivan, Ender Karaca, et al.Pageof 4