Pros and cons for fluorescent in situ hybridization, karyotyping and next generation sequencing for diagnosis and follow-up of multiple myeloma von Ikbal Atli, E, Gurkan, H, Onur Kirkizlar, H, Atli, E, Demir, S, Yalcintepe, S, Kalkan, R, Demir, AM

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Prenatal diagnosis of a new case: De novo balanced non-Robertsonian translocation involving t(15;22)(p11.2;q11.2) von 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... von Özdemir, K, Gürkan, H, Demir, S, Atli, E, Özen, Y, Sezer, A, Tunçbilek, N, Çicin, İ

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EP17.12: Prenatal diagnosis of an 18p deletion presenting with omphalocele von Sutcu, H., Sayin, C.N., Uzun, I., Erzincan, S., Inan, C., Yener, C., Ates, S., Atli, E., Gürkan, H., Varol, F.G.

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A case with Emanuel syndrome: extra derivative 22 chromosome inherited from the mother von İkbal Atli, E, Gürkan, H, Vatansever, Ü, Ulusal, S, Tozkir, H

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P-47 Preimplantation genetic diagnosis for ARC syndrome von Karadayi, H, Atli, E, Aktas, C, Berkil, H, Ozon, Y.H, Budak, E, Caferler, J

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P-38 Preimplantation genetic diagnosis for nemaline myopathy von Atli, E, Karadayi, H, Arslan, A, Berkil, H, Caferler, J, Ozen, C, Ozon, Y.H

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P-37 Preimplantation genetic diagnosis for hypoparathyroidism–deafness-renal dysplasia syndrome von Karadayi, H, Atli, E, Arslan, A, Caferler, J, Ozon, Y.H, Berkil, H, Bahce, M

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P-46 Preimplantation genetic diagnosis for glutaric aciduria type II von Atli, E, Karadayi, H, Aktas, C, Caferler, J, Ozon, Y.H, Sertyel, A, Berkil, H

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O-21 Preimplantation genetic diagnosis for single gene disorders applied in GENETIKS Laboratory von Ozon, Y.H, Karadayi, H, Atli, E, Caferler, J, Bahce, M, Berkil, H

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P-39 Preimplantation genetic diagnosis for epidermolysis bullosa von Karadayi, H, Atli, E, Aktas, C, Caferler, J, Berkil, H, Bahce, M, Ozon, Y.H

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P-44 Preimplantation genetic diagnosis for glycine encephalopathy von Atli, E, Karadayi, H, Aktas, C, Caferler, J, Ozon, Y.H, Bahce, M, Berkil, H

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The possible role of epigenetics in the etiology of hypospadias von S, Yıldız, I, Inanç, D, Zhuri, E, Atlı, D, Avlan

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P-43 Preimplantation genetic diagnosis for hereditary motor and sensory neuropathy type 1 von Karadayi, H, Atli, E, Aktas, C, Berkil, H, Ozon, Y.H, Ulug, A.A, Ulug, M, Caferler, J

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P-41 Preimplantation genetic diagnosis for lamellar ichthyosis type 2 von Atli, E, Karadayi, H, Aktas, C, Berkil, H, Ulug, M, Ulug, A.A, Caferler, J, Ozon, Y.H

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Does neuromuscular electrical stimulation have an effect on disabiliy, pain, abdominal and lumbar muscle thickness in chronic low back pain? von Atli, E., Karagözoğlu Coşkunsu, D., Ozyemisci Taskıran, O., Turan, Z.

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A 9-year-old-girl with Phelan McDermid Syndrome, who had been diagnosed with an autism spectrum disorder von Görker, I, Gürkan, H, Demir Ulusal, S, Atlı, E, Ikbal Atlı, E

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Genetic analyses of the NF1 gene in Turkish neurofibromatosis type I patients and definition of three novel variants von Ulusal, SD, Gürkan, H, Atlı, E, Özal, SA, Çiftdemir, M, Tozkır, H, Karal, Y, Güçlü, H, Eker, D, Görker, I

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A 9-Year-Old-Girl with Phelan McDermid Syndrome, Who Had been Diagnosed with an Autism Spectrum Disorder von Görker, I, Gürkan, H, Demir Ulusal, S, Atlı, E, Ikbal Atlı, E

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Deletion of macro domain containing 2(MACRO D2) associated with transient hydrops fetalis von Uzun Çilingir, I., Sayin, N.C., Gurkan, H., Çiftdemir, N.A., Atlı, E., İnan, C., Erzincan, S., Sutcu, H., Vatansever, U., Varol, F.

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