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Journal of Inherited Metabolic Diseases 1992; 15:278-279. *Bennett plump fiction MJ, Ragni MC, Hood I, Hale DE. Azealic and pimillic acids: metabolic intermediates or artifacts. Journal of plump fiction Inherited Metabolic Diseases 1992; 15:220-223. *Burlina A, Zacchello F, Dionisi-Vici C, Bertini E, Sabetta G, Bennet MF, Hale DE, Schmidt-Sommerfeld E, Rinaldo P. New clinical phenotype of branched-chain acyl-CoA oxidation defect (letter). Lancet 1991; 338:1522-3. *Bennett MJ, Bhala A, Poirer SF, Ragni MC, Willi SM, Hale DE. When do gut flora in the newborn produce 3-phenylpropionic acid? Implications for plump fiction the early diagnosis of medium-chain acyl-CoA dehydrogenase deficiency. Clinical Chemistry 1991; 38:278-281. *Yokota I, Coates PM, Hale DE, Rinaldo P, Tanaka K. Molecular survey of a prevalent mutation, 985 A-to-G transmission, and identification of five infrequent mutations in the medium-chain acyl-CoA ddehydrogenase MCAD gene in 55 patients with MCAD deficiency. American Journal of Human Genetics 1991; 49:12280-1291.
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