A 9-year-old-girl with Phelan McDermid Syndrome, who had been diagnosed with an autism spectrum disorder

by Görker I, Gürkan H, Demir Ulusal S, Atlı E, Ikbal Atlı E
Published 2016-12-01

Pros and cons for fluorescent in situ hybridization, karyotyping and next generation sequencing for diagnosis and follow-up of multiple myeloma

by Ikbal Atli E, Gurkan H, Onur Kirkizlar H, Atli E, Demir S, Yalcintepe S, Kalkan R, Demir AM
Published 2021-03-01

A case with Emanuel syndrome: extra derivative 22 chromosome inherited from the mother

by İkbal Atli E, Gürkan H, Vatansever Ü, Ulusal S, Tozkir H
Published 2015-12-01

Prenatal diagnosis of a new case: De novo balanced non-Robertsonian translocation involving t(15;22)(p11.2;q11.2)

by Atli Eİ, Gurkan H, Atli E, Tozkir H, Varol GF, İnan C
Published 2018-12-01

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 t...

by Özdemir K, Gürkan H, Demir S, Atli E, Özen Y, Sezer A, Tunçbilek N, Çicin İ
Published 2021-03-01

Genetic analyses of the NF1 gene in Turkish neurofibromatosis type I patients and definition of three novel variants

by Ulusal SD, Gürkan H, Atlı E, Özal SA, Çiftdemir M, Tozkır H, Karal Y, Güçlü H, Eker D, Görker I
Published 2017-06-01