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• Cloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15.

  Phaneuf D, Labelle Y, Bérubé D, Arden K, Cavenee W, Gagné R, Tanguay RM. Phaneuf D, et al. Am J Hum Genet. 1991 Mar;48(3):525-35. Am J Hum Genet. 1991. PMID: 1998338 Free PMC article.
• Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I).

  Tanguay RM, Valet JP, Lescault A, Duband JL, Laberge C, Lettre F, Plante M. Tanguay RM, et al. Am J Hum Genet. 1990 Aug;47(2):308-16. Am J Hum Genet. 1990. PMID: 2378356 Free PMC article.
• Liver transplantation in two children with tyrosinaemia type I: biochemical aspects.

  Riudor E, Ribes A, Lloret J, Friden J, Holme E, Jakobs C, Martinez Ibanez V. Riudor E, et al. J Inherit Metab Dis. 1991;14(3):281-4. doi: 10.1007/BF01811682. J Inherit Metab Dis. 1991. PMID: 1770775 No abstract available.
• Fumarylacetoacetase measurement as a mass-screening procedure for hereditary tyrosinemia type I.

  Laberge C, Grenier A, Valet JP, Morissette J. Laberge C, et al. Am J Hum Genet. 1990 Aug;47(2):325-8. Am J Hum Genet. 1990. PMID: 2378358 Free PMC article.
• Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus material.

  Kvittingen EA, Guibaud PP, Divry P, Mandon G, Rolland MO, Domenichini Y, Jakobs C, Christensen E. Kvittingen EA, et al. Eur J Pediatr. 1986 Apr;144(6):597-8. doi: 10.1007/BF00496047. Eur J Pediatr. 1986. PMID: 3709578 No abstract available.