Subject
Genetics (clinical),Genetics
Reference23 articles.
1. Andresen BS, Dobrowolski SF, O'Reilly L, et al (2001) Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency. Am J Hum Genet 68: 1408–1418.
2. Annual Report, Indiana State Department of Health available at: http://www.state.in.us/isdh/programs/nbs/NBSStatistics.htm.Accessed 24 August 2005
3. Bodamer O, Pollitt RJ (2005) Newborn screening and MCAD. Workshop results. 37th European Metabolic Group Meeting, Prague, Milupa, Friedrichsdorf.
4. 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.
5. Derks TG, Duran M, Waterham HR, Reijngoud DJ, Ten Kate LP, Smit GP (2005) The difference between observed and expected prevalence of MCAD deficiency in The Netherlands: a genetic epidemiological study. Eur J Hum Genet 13: 947–952.
Cited by
84 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