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Galactosemia Screening with Low False-Positive Recall Rate: The Swedish Experience
Newborn screening was implemented in the 1960s with screening for phenylketonuria (PKU). In the same decade, it became possible to screen for classical galactosemia, a rare autosomal recessive inherited disorder, which is potentially life threatening if not treated. While newborn screening for PKU h...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3509849/ https://ncbi.nlm.nih.gov/pubmed/23430863 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2011_59 |
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