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Clinical Utility of the Addition of Molecular Genetic Testing to Newborn Screening for Sickle Cell Anemia

Sickle cell disease (SCD) is a group of related yet genetically complex hemoglobinopathies. Universal newborn screening (NBS) for SCD is performed in the United States and many other nations. Classical, protein-based laboratory methods are often adequate for the diagnosis of SCD but have specific li...

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Detalles Bibliográficos
Autores principales:	Shook, Lisa M., Haygood, Deidra, Quinn, Charles T.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631351/ https://www.ncbi.nlm.nih.gov/pubmed/34859003 http://dx.doi.org/10.3389/fmed.2021.734305

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