Hoischen, A., van Bon, B. W. M., Rodríguez-Santiago, B., Gilissen, C., Vissers, L. E. L. M., de Vries, P., . . . de Vries, B. B. B. A. (2011). De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome. Nature genetics, 43(8), 729-731. https://doi.org/10.1038/ng.868
Chicago Style (17th ed.) CitationHoischen, Alexander, et al. "De Novo Nonsense Mutations in ASXL1 Cause Bohring-Opitz Syndrome." Nature Genetics 43, no. 8 (2011): 729-731. https://doi.org/10.1038/ng.868.
MLA (9th ed.) CitationHoischen, Alexander, et al. "De Novo Nonsense Mutations in ASXL1 Cause Bohring-Opitz Syndrome." Nature Genetics, vol. 43, no. 8, 2011, pp. 729-731, https://doi.org/10.1038/ng.868.
Warning: These citations may not always be 100% accurate.