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dc.contributor.authorRu-Lai, Yang-
dc.contributor.authorGu-Ling, Qian-
dc.contributor.authorDing-Wen, Wu-
dc.date.accessioned2023-03-21T01:29:28Z-
dc.date.available2023-03-21T01:29:28Z-
dc.date.issued2023-
dc.identifier.urihttps://link.springer.com/article/10.1007/s12519-022-00670-x-
dc.identifier.urihttps://dlib.phenikaa-uni.edu.vn/handle/PNK/7004-
dc.descriptionCC BYvi
dc.description.abstractNewborn screening (NBS) is an important and successful public health program that helps improve the long-term clinical outcomes of newborns by providing early diagnosis and treatment of certain inborn diseases. The development of next-generation sequencing (NGS) technology provides new opportunities to expand current newborn screening methodologies.vi
dc.language.isoenvi
dc.publisherSpringervi
dc.subjectNewborn screeningvi
dc.subjectnext-generation sequencingvi
dc.titleA multicenter prospective study of next-generation sequencing-based newborn screening for monogenic genetic diseases in Chinavi
dc.typeBookvi
Appears in CollectionsOER- Y học- Điều dưỡng

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