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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Bibliografiska uppgifter
I publikationen:Am J Hum Genet
Huvudupphovsmän: Roman, Tamara S., Crowley, Stephanie B., Roche, Myra I., Foreman, Ann Katherine M., O’Daniel, Julianne M., Seifert, Bryce A., Lee, Kristy, Brandt, Alicia, Gustafson, Chelsea, DeCristo, Daniela M., Strande, Natasha T., Ramkissoon, Lori, Milko, Laura V., Owen, Phillips, Roy, Sayanty, Xiong, Mai, Paquin, Ryan S., Butterfield, Rita M., Lewis, Megan A., Souris, Katherine J., Bailey, Donald B., Rini, Christine, Booker, Jessica K., Powell, Bradford C., Weck, Karen E., Powell, Cynthia M., Berg, Jonathan S.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Elsevier 2020
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Article
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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