Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol

被引：0
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作者：
Stephan Lobitz
Claudia Frömmel
Annemarie Brose
Oliver Blankenstein
Charles Turner
R. Neil Dalton
Yvonne Daniel
Jeannette Klein
机构：
[1] Gemeinschaftsklinikum Mittelrhein,Department of Pediatric Hematology and Oncology
[2] Alexianer St. Hedwig Krankenhaus,Department of Laboratory Medicine
[3] Charité – Universitätsmedizin Berlin,Newborn Screening Laboratory
[4] Evelina London Children’s Hospital,SpOtOn Clinical Diagnostics
来源：
Annals of Hematology | 2022年 / 101卷
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页码：1859 / 1860
页数：1
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