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3. Dicarboxylicaciduria during ketotic phases in various types of glycogen storage disease;Pettersen, J.E.; Wixnes, A.;Acta Pediatr Scand,1981
4. Gas chromatography-massspectrometry (GC-MS) diagnosis of two cases of medium chain acyl-coA dehydrogenase deficiency;Divry, P.; Vianey-Liaud, C.; Cotte, J.;J Inherited Metab Dis,1984
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