APA ציטוט

Berko, E. R., Cho, M. T., Eng, C., Shao, Y., Sweetser, D. A., Waxler, J., . . . Chung, W. K. (2016). De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. J Med Genet.

Citação norma Chicago

Berko, Esther R., et al. "De Novo Missense Variants in HECW2 Are Associated With Neurodevelopmental Delay and Hypotonia." J Med Genet 2016.

ציטוט MLA

Berko, Esther R., et al. "De Novo Missense Variants in HECW2 Are Associated With Neurodevelopmental Delay and Hypotonia." J Med Genet 2016.