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Newborn screening for genetic disorders: Current status and prospects for the future

Newborn screening (NBS) is a public health service aimed at identifying infants with severe genetic disorders, thus providing effective treatment early enough to prevent or ameliorate the onset of symptoms. Current NBS uses biochemical analysis of dried blood spots, predominately with time‐resolved...

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Detalles Bibliográficos
Autores principales: Ding, Si, Han, Lianshu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789938/
https://www.ncbi.nlm.nih.gov/pubmed/36582269
http://dx.doi.org/10.1002/ped4.12343