Genetic analyses of the NF1 gene in Turkish neurofibromatosis type I patients and definition of three novel variants
Ulusal, SD, Gürkan, H, Atlı, E, Özal, SA, Çiftdemir, M, Tozkır, H, Karal, Y, Güçlü, H, Eker, D, Görker, I
Prenatal diagnosis of a new case: De novo balanced non-Robertsonian translocation involving t(15;22)(p11.2;q11.2)
Atli, Eİ, Gurkan, H, Atli, E, Tozkir, H, Varol, GF, İnan, C
Next-Generation Sequencing Infertility Panel in Turkey: First Results
Ikbal Atli, E, Yalcintepe, S, Atli, E, Demir, S, Gurkan, H
Investigation of the relationship of TNFRSF11A gene polymorphisms with breast cancer development and metastasis risk in patients with BRCA1 or BRCA2 pathogenic variants living in the Trakya region of Turkey
Özdemir, K, Gürkan, H, Demir, S, Atli, E, Özen, Y, Sezer, A, Tunçbilek, N, Çicin, İ
A 9-year-old-girl with Phelan McDermid Syndrome, who had been diagnosed with an autism spectrum disorder
Görker, I, Gürkan, H, Demir Ulusal, S, Atlı, E, Ikbal Atlı, E
Von Hippel-Lindau disease: the clinical manifestations and genetic analysis results of two cases from a single family
Kinyas, S, Ozal, SA, Guclu, H, Gurlu, V, Esgin, H, Gurkan, H
A case with Emanuel syndrome: extra derivative 22 chromosome inherited from the mother
İkbal Atli, E, Gürkan, H, Vatansever, Ü, Ulusal, S, Tozkir, H
Pros and cons for fluorescent in situ hybridization, karyotyping and next generation sequencing for diagnosis and follow-up of multiple myeloma
Ikbal Atli, E, Gurkan, H, Onur Kirkizlar, H, Atli, E, Demir, S, Yalcintepe, S, Kalkan, R, Demir, AM