APA (7th ed.) Citation

RG, F., M, P., K, S., K, B., A, R., SB, W., & JA, M. (2022). A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. Genes, 13(12), . https://doi.org/10.3390/genes13122191

Chicago Style (17th ed.) Citation

RG, Feichtinger, Preisel M, Steinbrücker K, Brugger K, Radda A, Wortmann SB, and Mayr JA. "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). https://doi.org/10.3390/genes13122191.

MLA (9th ed.) Citation

RG, Feichtinger, 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, https://doi.org/10.3390/genes13122191.