Molecular diagnostic update in hereditary hemolytic anemia and neonatal hyperbilirubinemia
Author:
Affiliation:
1. Department of Pathology University of Utah Health Salt Lake City Utah
2. ARUP Laboratories Salt Lake City Utah
3. Division of Neonatology and Hematology/Oncology University of Utah Health Salt Lake City Utah
Publisher
Wiley
Subject
Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijlh.13014
Reference48 articles.
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3. Gilbert syndrome and glucose‐6‐phosphate dehydrogenase deficiency: a dose‐dependent genetic interaction crucial to neonatal hyperbilirubinemia;Kaplan M;Proc Natl Acad Sci USA,1997
4. New insights on hereditary erythrocyte membrane defects;Andolfo I;Haematologica,2016
5. Hereditary stomatocytosis: an underdiagnosed condition;Andolfo I;Am J Hematol,2018
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