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