Wiedemann-Steiner Syndrome as a Differential Diagnosis of Cornelia de Lange Syndrome Using Targeted Next-Generation Sequencing: A Case Report von Demir, Selma, Gürkan, Hakan, Öz, Veysel, Yalçıntepe, Sinem, Atlı, Emine İ., Atlı, Engin

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A Rare Case of Mosaic Unbalanced Non-Robertsonian Translocation Involving Chromosomes 15 and 22 with Congenital Abnormalities in Monozygotic Twins von Atli, Emine I., Atli, Engin, Yalcintepe, Sinem, Gurkan, Hakan

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Distal 3p Duplication and 22q13.3 Deletion with Severe Hypotonia Originating from a Paternal Balanced Translocation (3;22) von Yalcintepe, Sinem, Atli, Emine I., Atli, Engin, Demir, Selma, Ciftdemir, Nukhet A., Duran, Ridvan, Ozdemir, Janset, Gurkan, Hakan

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Wiedemann-Steiner Syndrome as a Differential Diagnosis of Cornelia de Lange Syndrome Using Targeted Next-Generation Sequencing: A Case Report von Demir, Selma, Gürkan, Hakan, Öz, Veysel, Yalçıntepe, Sinem, Atlı, Emine I, Atlı, Engin

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