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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 p23.3 deletion and 16q23.2-q24.3 duplication detected by arrayCGH in a patient with intellectuel disability(Nature Publishing Group, 2019) Ozen, Y.; Gurkan, H.; Atli, E.; Atli, E. I.; Akurut, C.; Moustafa, N.; Demir, S.[Abstract Not Available]
