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Öğe 17q22 microdeletion detected by array-CGH leading to NOG-related symphalangism spectrum disorder (NOG-SSD)(Nature Publishing Group, 2019) Atli, E.; Gurkan, H.; Atli, E. I.; Ozen, Y.; Eker, D.; Akurut, C.; Demir, S.[Abstract Not Available]Öğe ArrayCGH analysis in patients with intellectual disability/developmental delay in Turkish Children living in Trakya Region(Nature Publishing Group, 2018) Gurkan, H.; Gorker, I.; Atli, E.; Atli, E. I.; Ulusal, S. Demir; Eker, D.; Tozkir, H.[Abstract Not Available]Öğe Combined Partial Trisomy 7q and Partial Monosomy 21q in a 6 Year Old Male Patient Phenotypic and Genotypic Findings(Nature Publishing Group, 2019) Atli, E. I.; Gurkan, H.; Atli, E.; Ozen, Y.; Gorker, I.; Eker, D.; Akurut, C.[Abstract Not Available]Öğe Different phenotype with 22q13.3 deletion syndrome in two patients(Nature Publishing Group, 2019) Gurkan, H.; Atli, E.; Atli, E.; Demir, S.; Ozen, Y.; Tozkir, H.; Eker, D.[Abstract Not Available]Öğe Genetic diagnosis of bone mineralisation disorders with Next Generation Sequencing and definition of five novel pathogenic variations(Nature Publishing Group, 2019) Tozkir, H.; Demir, S.; Gurkan, H.; Eker, D.; Atli, E.[Abstract Not Available]Öğe Screening for CALR gene mutations in Jak-2 V617F mutation negative patients with myeloproliferative neoplasms(Nature Publishing Group, 2018) Ulusal, S. Demir; Umit, E. G.; Gurkan, H.; Tozkir, H.; Baysal, M.; Goncu, E.; Eker, D.[Abstract Not Available]Öğe Screening for germline variations of cancer related genes in patients with the diagnosis of different cancers and hereditary cancer predisposition syndromes(Nature Publishing Group, 2019) Demir, S.; Tozkur, H.; Gurkan, H.; Atli, E.; Eker, D.; Tezel, H. A.; Sezer, Y. A.[Abstract Not Available]
