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Feichtinger RG, Preisel M, Steinbrücker K, Brugger K, Radda A, Wortmann SB, Mayr JA. A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. Genes. 2022; 13(12):2191. https://doi.org/10.3390/genes13122191

Feichtinger, René G., Martin Preisel, Katja Steinbrücker, Karin Brugger, Alexandra Radda, Saskia B. Wortmann, and Johannes A. Mayr. 2022. "A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome" Genes 13, no. 12: 2191. https://doi.org/10.3390/genes13122191

Feichtinger, R. G., Preisel, M., Steinbrücker, K., Brugger, K., Radda, A., Wortmann, S. B., & Mayr, J. A. (2022). A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. Genes, 13(12), 2191. https://doi.org/10.3390/genes13122191