Cite
McBean R, Liew YW, Wilson B, et al. Genotyping confirms inheritance of the rare At(a-) type in a case of haemolytic disease of the newborn. J Pathol Clin Res. 2015;2(1):53-5doi: 10.1002/cjp2.33.
McBean, R., Liew, Y. W., Wilson, B., Kupatawintu, P., Emthip, M., Hyland, C., & Flower, R. (2016). Genotyping confirms inheritance of the rare At(a-) type in a case of haemolytic disease of the newborn. The journal of pathology. Clinical research, 2(1), 53-5. https://doi.org/10.1002/cjp2.33
McBean, Rhiannon, et al. "Genotyping confirms inheritance of the rare At(a-) type in a case of haemolytic disease of the newborn." The journal of pathology. Clinical research vol. 2,1 (2016): 53-5. doi: https://doi.org/10.1002/cjp2.33
McBean R, Liew YW, Wilson B, Kupatawintu P, Emthip M, Hyland C, Flower R. Genotyping confirms inheritance of the rare At(a-) type in a case of haemolytic disease of the newborn. J Pathol Clin Res. 2015 Dec 11;2(1):53-5. doi: 10.1002/cjp2.33. eCollection 2016 Jan. PMID: 27499913; PMCID: PMC4858124.
Copy
Download .nbib