Atli, Emine I.Atli, EnginYalcintepe, SinemGurkan, Hakan2024-06-122024-06-1220201661-87691661-8777https://doi.org/10.1159/000505004https://hdl.handle.net/20.500.14551/20093Balanced de novo non-robertsonian translocations (non-RTs), which involve acrocentric chromosomes, are rare findings in clinical cytogenetics and may be associated with an abnormal phenotype. These translocations, detected by conventional karyotyping, are found in approximately 1:1,000 neonates. In most of these cases, one of the parents carries the same translocation. In this study, we report a rare non-RT involving chromosomes 15 and 22 defined as 45,XX,-22,der(15;22)t(15;22)/46,XX,der(15)t(15;22),der(22). To our knowledge, this is the first report of a non-RT t(15;22) with these breakpoints.en10.1159/000505004info:eu-repo/semantics/openAccessCopy Number VariationsDeletion SyndromeDysmorphologyFISHGenotype-Phenotype CorrelationMosaicismArray CGHAutismChromosomal Microarray Analysis22q11.2 DeletionDigeorge-SyndromeFeaturesChildArticle106320326Q4WOS:0005088457000052-s2.0-8507745090132021606Q4