APA (7th ed.) Citation

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

Chicago Style (17th ed.) Citation

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

MLA (9th ed.) Citation

Feichtinger, René G., et al. "A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome." Genes, vol. 13, no. 12, 2022, p. 2191, https://doi.org/10.3390/genes13122191.