APA (7th ed.) Citation

J, J., T, B., W, D., A, T., P, G., AL, B., . . . B, I. (2025). Heterozygous alterations of GTF2I at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorder. Journal of medical genetics. https://doi.org/10.1136/jmg-2024-110471

Chicago Style (17th ed.) Citation

J, Jury, et al. "Heterozygous Alterations of GTF2I at the Williams-Beuren Syndrome's Locus Cause a Neurodevelopmental Disorder." Journal of Medical Genetics 2025. https://doi.org/10.1136/jmg-2024-110471.

MLA (9th ed.) Citation

J, Jury, et al. "Heterozygous Alterations of GTF2I at the Williams-Beuren Syndrome's Locus Cause a Neurodevelopmental Disorder." Journal of Medical Genetics, 2025, https://doi.org/10.1136/jmg-2024-110471.