Funder
Florida Department of Heath State Appropriation, Cornelia T. Bailey Foundation, Sanford Health and Nicklaus Children’s Health Care Foundation.
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology,Genetics,Molecular Medicine
Reference41 articles.
1. Ontario Health (Quality). Genome-wide sequencing for unexplained developmental disabilities or multiple congenital anomalies: a health technology assessment. Ont Health Technol Assess Ser. 2020;20:1–178.
2. Lionel AC, Costain G, Monfared N, Walker S, Reuter MS, Hosseini SM, et al. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test. Genet Med. 2018;20:435–43. https://doi.org/10.1038/gim.2017.119.
3. Friedman JM, Bombard Y, Cornel MC, Fernandez CV, Junker AK, Plon SE, et al. Genome-wide sequencing in acutely ill infants: genomic medicine’s critical application? Genet Med. 2019;21:498–504. https://doi.org/10.1038/s41436-018-0055-z.
4. Alam K, Schofield D. Economic evaluation of genomic sequencing in the paediatric population: a critical review. Eur J Hum Genet. 2018;26:1241–7. https://doi.org/10.1038/s41431-018-0175-6.
5. Farnaes L, Hildreth A, Sweeney NM, Clark MM, Chowdhury S, Nahas S, et al. Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization. npj Genom Med. 2018;3:10. https://doi.org/10.1038/s41525-018-0049-4.
Cited by
14 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献