Funder
U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute
U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference71 articles.
1. Ng SB, Buckingham KJ, Lee C, Bigham AW, Tabor HK, Dent KM, et al. Exome sequencing identifies the cause of a mendelian disorder. Nat Genet. 2010;42:30–5.
2. Genomics Education Programme. Genomic medicine. 2021. https://www.genomicseducation.hee.nhs.uk/glossary/genomic-medicine/.
3. National Human Genome Research Institute. Genomics and medicine. 2020. https://www.genome.gov/health/Genomics-and-Medicine.
4. Kingsmore SF, Cole FS. The role of genome sequencing in neonatal intensive care units. Annu Rev Genomics Hum Genet. 2022;23:427–48.
5. Saunders CJ, Miller NA, Soden SE, Dinwiddie DL, Noll A, Alnadi NA, et al. Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. Sci Transl Med. 2012;4:154ra35.
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