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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 Four novel pathogenic variants in TSC2 gene of Turkish patients with tuberous sclerosis complex(Nature Publishing Group, 2018) Tozkir, H.; Ulusal, S. Demir; Gurkan, H.; Atli, E.; Karal, Y.; Karasalihoglu, S.[Abstract Not Available]Öğe A nine year old girl with phelan mc dermid syndrome, who had been diagnosed with autism spectrum disorder(Springer, 2015) Gorker, I.; Gurkan, H.; Ulusal, S. Demir[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]
