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 ChicagoJohnson, Ben, et al. "Whole Exome Sequencing Identifies Genetic Variants in Inherited Thrombocytopenia With Secondary Qualitative Function Defects." Haematologica 2016.
Cita MLAJohnson, Ben, et al. "Whole Exome Sequencing Identifies Genetic Variants in Inherited Thrombocytopenia With Secondary Qualitative Function Defects." Haematologica 2016.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.