A New Set of Clinical Tools for Physicians
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-80100-7_9
Reference9 articles.
1. Namboth S, Thevenon J, et al. Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis. Genet Med. 2018;20(6):645–54.
2. Ginsburg D. Genetics and genomics to the clinic: a long road ahead. Cell. 2011;147:17–9.
3. Burnette R, Simmons LA, Snyderman R. Personalized health care as a pathway for the adoption of genomic medicine. J Personal Med. 2012;2:232–40.
4. Vora NL, Gilmore K, Brandt A, Gustafson C, Strande N, et al. An approach to integrating exome sequencing for fetal structural anomalies into clinical practice. 2020;22(5):954–61.
5. Reuter MS, Chaturvedi RR, Joblin RK. The cardiac genome clinic: implementing genome sequencing in pediatric heart disease. Genet Med. 2020;22(6):1015–24.
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