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Genomic newborn screening for rare diseases

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Year: 2023
Type: review
Source: Nature Reviews Genetics
DOI: 10.1038/s41576-023-00621-w
Authors: Zornitza Stark, Richard H. Scott
Institutions: The University of Melbourne, Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Australian Genomics Health Alliance, Great Ormond Street Hospital, Genomics England, University College London
Language: English

Topic: Genomics and Rare Diseases
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W4382631903
FWCI: 8.272
Cites: 141
Cited by: 246
Related to: 10
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