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Danpure CJ, Purdue PE (1994) Primary hyperoxaluria. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic basis of inherited disease, 7th edn. McGraw-Hill (in press)
Purdue PE, Lumb MJ, Allsop J, Danpure CJ (1991) An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1. Hum genet 87: 394–396
Danpure CJ, Birdsey GM, Rumsby G, Lumb MJ, Purdue PE, Allsop J (1994) Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine: glyoxylate aminotransferase gene. Hum Genet 94: 55–64
Danpure CJ, Jennings PR, Fryer P, Purdue PE, Allsop J (1994) Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity. J Inherited Metab Dis 17: 487–499
Danpure CJ, Jennings PR, Penketh RJ, Wise PJ, Cooper PJ, Rodeck CH (1989) Fetal liver alanine: glyoxylate aminotransferase and the prenatal diagnosis of primary hyperoxaluria type 1. Prenat Diagn 9: 271–281
Danpure CJ, Cooper PJ, Jennings PR, Wise PJ, Penketh RJ, Rodeck CH (1989) Enzymatic prenatal diagnosis of primary hyperoxaluria type 1: potential and limitations. J Inherited Metab Dis 12 [Suppl 2]: 286–288
Cooper PJ, Danpure CJ, Penketh RJ (1989) Prenatal differentiation of primary hyperoxaluria type 1 phenotypes in the first trimester using immuno-electron microscopy. Clin Sci 76 [Suppl 20]: 13
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Danpure, C.J. Ask the expert. Pediatr Nephrol 10, 190 (1996). https://doi.org/10.1007/BF00862073
- Primary hyperoxaluria
- Prenatal diagnosis