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Comment
. 2001 Apr 28;322(7293):1062.

Screening for medium chain acyl-CoA dehydrogenase deficiency is being evaluated

Comment

Screening for medium chain acyl-CoA dehydrogenase deficiency is being evaluated

S Grosse. BMJ. .
No abstract available

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References

    1. Tanner S, Sharrard M, Cleary M, Walter J, Wraith E, Lee P, et al. Screening for medium chain acyl-CoA dehydrogenase deficiency has still not been evaluated. BMJ. 2001;322:112. . (13 January.) - PMC - PubMed
    1. Pollitt RJ, Green A, McCabe CJ, Booth A, Cooper NJ, Leonard JV, et al. Neonatal screening for inborn errors of metabolism: cost, yield and outcome. Health Technol Assess. 1997;1(7):1–202. - PubMed
    1. Seymour CA, Thomason MJ, Chalmers RA, Addison MJ, Bain MD, Cockburn F, et al. Neonatal screening for inborn errors of metabolism: a systematic review. Health Technol Assess. 1997;1(11):1–95. - PubMed
    1. Wang SS, Fernhoff PM, Hannon WH, Khoury MJ. Medium chain acyl-coA dehydrogenase deficiency (MCADD) Genet Med. 1999;1:332–339. - PubMed
    1. Atkinson K, Zuckerman B, Sharfstein JM, Levin D, Blatt RM, Koh HK. A public health response to emerging technology: expansion of the Massachusetts newborn screening program. Public Health Rep (in press). - PMC - PubMed

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