Next-Generation Sequencing Infertility Panel in Turkey: First Results by Ikbal Atli E, Yalcintepe S, Atli E, Demir S, Gurkan H

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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

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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

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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

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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

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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

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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

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