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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Bibliographic Details
Published in:Am J Hum Genet
Main Authors: 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.
Format: Artigo
Language:Inglês
Published: Elsevier 2020
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Online Access: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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