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Amedeo Smart

Independent Medical Education


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Lobitz S, Frommel C, Brose A, Blankenstein O, et al. Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol. Ann Hematol 2022;101:1859-1860.
PMID: 35293609


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