Newborn Screening in the Era of Precision Medicine-Reference-Cited by-同舟云学术

Newborn Screening in the Era of Precision Medicine

Published:2017 Issue: Volume: Page:47-61
ISSN:0065-2598
Container-title:Advances in Experimental Medicine and Biology
language:
Short-container-title:

Author:

Yang Lan,Chen Jiajia,Shen Bairong

Publisher

Springer Singapore

Link

http://link.springer.com/content/pdf/10.1007/978-981-10-5717-5_3

Reference43 articles.

1. National newborn screening report. National Newborn Screening and Genetics Resource Center. 2013. http://genes-rus.uthscsa.edn/resources/newborn/00/ch2_complete.pdf

2. Recommended Uniform Screening Panel of the Secretary’s Advisory Committee on Heritable Disorders in Newborns and Children. Secretary’s Advisory Committee on Heritable Disorders in Newborns and Children. 2012. http://www.hrsa.gov/advisorycommittees/mchbadvisory/heritabledisorders/recommendedpanel/index.html

3. Exe N, et al. Genetic testing stories. Washington, DC: Genetic Alliance; 2006.

4. Wright C. Next steps in the sequence: the implications of whole genome sequencing for health in the UK. Cambridge: PHG Foundation; 2011.

5. Scaria V. Personal genomes to precision medicine. Mol Cytogenet. 2014;7(Suppl 1 Proceedings of the International Conference on Human):I28.

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