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The Application of Clinical Genetics Volume 17, 2024 - Issue
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CASE REPORT

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

Gabriela RękaIndependent Laboratory of Genetic Diagnostics of the Second Chair of Pediatrics, Medical University of Lublin, Lublin, PolandCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0001-9728-5281
ORCID Icon,
Katarzyna WojciechowskaIndependent Laboratory of Genetic Diagnostics of the Second Chair of Pediatrics, Medical University of Lublin, Lublin, Poland
&
Monika LejmanIndependent Laboratory of Genetic Diagnostics of the Second Chair of Pediatrics, Medical University of Lublin, Lublin, Poland
Pages 117-124 | Received 23 Feb 2024, Accepted 25 Jun 2024, Published online: 14 Jul 2024

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