Publications by authors named "Alexandra Radda"

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A Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome.
René G Feichtinger, Martin Preisel, Katja Steinbrücker, Karin Brugger, Alexandra Radda

Genes (Basel)· November 2022

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