Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus material
- 1 April 1986
- journal article
- letter
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 144 (6), 597-598
- https://doi.org/10.1007/bf00496047
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Prenatal diagnosis of tyrosinaemia type I by use of stable isotope dilution mass spectrometryEuropean Journal of Pediatrics, 1985
- EARLY PRENATAL DIAGNOSIS OF HEREDITARY TYROSINAEMIAThe Lancet, 1985
- Prenatal Diagnosis of Hereditary Tyrosinemia by Determination of Fumarylacetoacetase in Cultured Amniotic Fluid CellsPediatric Research, 1985
- POSSIBILITIES FOR TREATMENT AND FOR EARLY PRENATAL DIAGNOSIS OF HEREDITARY TYROSINAEMIAThe Lancet, 1985
- Deficient Fumarylacetoacetate Fumarylhydrolase Activity in Lymphocytes and Fibroblasts from Patients with Hereditary TyrosinemiaPediatric Research, 1983
- Prenatal diagnosis of hereditary tyrosinaemia: Measurement of succinylacetone in amniotic fluidPrenatal Diagnosis, 1982
- GC-MS identification of urinary succinylacetone in two cases of hereditary tyrosinaemiaJournal of Inherited Metabolic Disease, 1982
- On the enzymic defects in hereditary tyrosinemia.Proceedings of the National Academy of Sciences, 1977