Author:
Urv Tiina K.,Parisi Melissa A.
Publisher
Springer International Publishing
Reference42 articles.
1. Bailey DB Jr, Gehtland L (2015) Newborn screening: evolving challenges in an era of rapid discovery. JAMA 313(15):1511–1512
2. Baker MW, Laessig RH, Katcher ML, Routes JM, Grossman WJ, Verbsky J et al (2010) Implementing routine testing for severe combined immunodeficiency within Wisconsin’s newborn screening program. Public Health Rep 125(Suppl 2):88–95
3. Berg JS, Agrawal PB, Bailey DB Jr, Beggs AH, Brenner SE, Brower AM et al (2017) Newborn sequencing in genomic medicine and public health. Pediatrics 139(2):e20162252
4. Berry SA (2015) Newborn screening. Clin Perinatol 42(2):441–453. x
5. Botkin J (2016) Pilot study workgroup–report. In: HHS (ed) Advisory committee on heritable disorders in newborns and children, pp 6–10. Available from: https://www.hrsa.gov/advisorycommittees/mchbadvisory/heritabledisorders/meetings/2016/eleventh/achdncmay2016meetingminutes.pdf
Cited by
22 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