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Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1

Stephan Lobitz1, Claudia Frömmel2, Annemarie Brose3

  • 1Department of Pediatric Hematology and Oncology, Gemeinschaftsklinikum Mittelrhein, Koblenzer Strasse 115-155, 56073, Koblenz, Germany. Stephan.Lobitz@gk.de.

Annals of Hematology
|March 16, 2022
PubMed
Abstract

No abstract available in PubMed .

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