3. Chace DH, Kalas TA, Naylor EW. 2002; The application of tandem mass spectrometry to neonatal screening for inherited disorders of intermediary metabolism. Annu Rev Genomics Hum Genet. 3:17–45. DOI:
10.1146/annurev.genom.3.022502.103213. PMID:
12142359.
Article
4. Wilcken B, Wiley V, Hammond J, Carpenter K. 2003; Screening newborns for inborn errors of metabolism by tandem mass spectrometry. N Engl J Med. 348:2304–12. DOI:
10.1056/NEJMoa025225. PMID:
12788994.
Article
5. Zytkovicz TH, Fitzgerald EF, Marsden D, Larson CA, Shih VE, Johnson DM, et al. 2001; Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening Program. Clin Chem. 47:1945–55. DOI:
10.1093/clinchem/47.11.1945. PMID:
11673361.
6. Lee B, Heo WY, Kim JA, Lee HS, Hwang N, Park HD, et al. 2023; Comprehensive evaluation of the NeoBase 2 non-derivatized MSMS assay with exploration of analytes with significantly different levels between term and preterm neonates. Ann Lab Med. 43:153–66. DOI:
10.3343/alm.2023.43.2.153. PMID:
36281509.
Article