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Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project
Newborn screening (NBS) was established as a public health program in the 1960s and is crucial for facilitating detection of certain medical conditions in which early intervention can prevent serious, life-threatening health problems. Genomic sequencing can potentially expand the screening for rare...
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| I publikationen: | Am J Hum Genet |
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| Huvudupphovsmän: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Elsevier
2020
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7536575/ https://ncbi.nlm.nih.gov/pubmed/32853555 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2020.08.001 |
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