Hereditary Metabolic Diseases
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-24958-7_31
Reference13 articles.
1. American Academy of Pediatrics Newborn Screening Task Force (2000) Serving the family from birth to medical home. Newborn screening a blue print for the future. A call for a national agenda on state newborn screening programs. Pediatrics 106(Suppl 2):389–422
2. American College of Medical Genetics Newborn Screening Expert Group (2006) Newborn Screening toward a uniform screening panel and system. Executive summary. Pediatrics 117:S296–S307
3. Carroll AE, Downs SM (2006) Comprehensive cost-utility analysis of newborn screening strategies. Pediatrics 117:S287–S295
4. CDC (2012) Good laboratory practices for biochemical genetic testing and newborn screening for inherited metabolic disorders. MMWR Recomm Rep 61(2)
5. Chace DH, Kalas TA, Naylor EW (2003) Use of tandem mass spectrometry for multianalyte screening of dried blood specimens from newborns. Clin Chem 49:1797–1817
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