First-trimester prenatal diagnosis of tyrosinemia type I by amniotic fluid succinylacetone determination
- 1 February 1990
- journal article
- Published by Wiley in Prenatal Diagnosis
- Vol. 10 (2), 133-134
- https://doi.org/10.1002/pd.1970100210
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Prenatal Diagnosis of Inherited Metabolic Disorders by Stable Isotope Dilution GC-MS Analysis of Metabolites in Amniotic Fluid: Review of Four Years ExperienceJournal of Inherited Metabolic Disease, 1989
- Stable isotope dilution analysis of succinylacetone using electron capture negative ion mass fragmentography: an accurate approach to the pre- and neonatal diagnosis of hereditary tyrosinemia type IClinica Chimica Acta; International Journal of Clinical Chemistry, 1988
- TRANSABDOMINAL CHORION VILLUS BIOPSY: 100 CONSECUTIVE CASESThe Lancet, 1987
- EARLY PRENATAL DIAGNOSIS OF HEREDITARY TYROSINAEMIAThe Lancet, 1985