Failure or delay in diagnosing Fanconi anemia--a well-defined genetic disorder by Deniz Aslan

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"Silent" β-thalassemia mutation (promoter nt-101 C > T) with increased hemoglobin A by Deniz Aslan

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Formulas for the Detection β-Thalassemia Carriers Are Affected by Changes in Red Cell Parameters by Deniz Aslan

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Molecular diagnosis of Fanconi anemia with next-generation sequencing in a case with subtle signs and a negative chromosomal breakage test by Deniz Aslan, Najim Ameziane, Johan P De Winter

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Recessive congenital methemoglobinemia in immediate generations by Deniz Aslan, Gülsan Türköz-Sucak, Melanie Joan Percy

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Trauma as a risk factor for thrombosis in children: a report of three cases by Emel Ozyürek, Nesrin Beşbaş, Deniz Aslan, Aytemiz Gürgey

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DNA damage in children with β-thalassemia minor: genotoxicity assessment by comet assay by Deniz Menderes, Esra Emerce, Tayfun Göktaş, Gonca Çakmak, Deniz Aslan

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