Author:
Leonard J V,Seakins J W,Bartlett K,Hyde J,Wilson J,Clayton B
Subject
Pediatrics, Perinatology and Child Health
Reference24 articles.
1. A new inborn error of metabolismLancet;crotonylglycinuria,1970
2. Biotin responsive 3-methylcrotonylglycinuria;Gompertz, D.; H, Draffan G.; L, Watts J.; Hull, D.;Lancet,1971
3. Child with a defect in leucine metabolism associated with fhydroxyisovaleric aciduria and,-methylcrotonylglycinuria;Gompertz, D.; Bartlett, K.; Blair, D.; M, Stern C.M.;Arch Dis Child,1973
4. Massive excretion of 2-oxoglutaric acid and 3-hydroxyisovaleric acid in a patient with deficiency of 3-methylcrotonyl CoA carboxylase;A, Finnie M.D.; K, Cottrall; T, Seakins J.W.; W, Snedden;Clin Chim Acta,1976
5. Organic aciduria. Treatable cause of floppy infant syndrome;R, Keeton B.; A, Moosa;Arch Dis Child,1976
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