APA aipamena

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.

Chicago Style aipamena

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

MLA aipamena

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