Cita APA

Johnson, B., Lowe, G. C., Futterer, J., Lordkipanidzé, M., MacDonald, D., Simpson, M. A., . . . Morgan, N. V. (2016). Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects. Haematologica.

Citación estilo Chicago

Johnson, Ben, et al. "Whole Exome Sequencing Identifies Genetic Variants in Inherited Thrombocytopenia With Secondary Qualitative Function Defects." Haematologica 2016.

Cita MLA

Johnson, Ben, et al. "Whole Exome Sequencing Identifies Genetic Variants in Inherited Thrombocytopenia With Secondary Qualitative Function Defects." Haematologica 2016.