Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome.

MLA

Van Houdt, Jeroen K. J., et al. “Heterozygous Missense Mutations in SMARCA2 Cause Nicolaides-Baraitser Syndrome.” Nature Genetics, vol. 44, no. 4, Feb. 2012, p. 445. EBSCOhost, https://doi.org/10.1038/ng.1105.

APA

Van Houdt, J. K. J., Nowakowska, B. A., Sousa, S. B., van Schaik, B. D. C., Seuntjens, E., Avonce, N., Sifrim, A., Abdul-Rahman, O. A., van den Boogaard, M.-J. H., Bottani, A., Castori, M., Cormier-Daire, V., Deardorff, M. A., Filges, I., Fryer, A., Fryns, J.-P., Gana, S., Garavelli, L., Gillessen-Kaesbach, G., … Vermeesch, J. R. (2012). Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome. Nature Genetics, 44(4), 445. https://doi.org/10.1038/ng.1105

Chicago

Van Houdt, Jeroen K J, Beata Anna Nowakowska, Sérgio B Sousa, Barbera D C van Schaik, Eve Seuntjens, Nelson Avonce, Alejandro Sifrim, et al. 2012. “Heterozygous Missense Mutations in SMARCA2 Cause Nicolaides-Baraitser Syndrome.” Nature Genetics 44 (4): 445. doi:10.1038/ng.1105.