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July 1, 2024The Application of Clinical GeneticsOpen Access

Rare Case of de Novo 2p15 Microdeletion Syndrome with Deletion Covering XPO1 and USP34 Genes Diagnosed in a Child – A Case Report

Gabriela Ręka Katarzyna Wojciechowska Monika Lejman

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Abstract

2p15p16.1 microdeletion syndrome was described for the first time in 2007. The size of the microdeletion is variable and encompasses several genes, like

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Cite This Study

Ręka et al. (2024) studied this question.

synapsesocial.com/papers/68e6237eb6db6435875b577e https://doi.org/10.2147/tacg.s465575

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