Utility of whole-genome sequencing for detection of newborn...

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Genetics in Medicine 2015 / 09

Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates

Bodian, Dale L., Klein, Elisabeth, Iyer, Ramaswamy K., Wong, Wendy S. W., Kothiyal, Prachi, Stauffer, Daniel, Huddleston, Kathi C., Gaither, Amber D., Remsburg, Irina, Khromykh, Alina, Baker, Robin L.
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Language:
english
Journal:
Genetics in Medicine
DOI:
10.1038/gim.2015.111
Date:
September, 2015
File:
PDF, 692 KB
english, 2015
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