An example of rapid prenatal diagnosis of Fabry's disease usingmicrotechniques
- 23 April 1974
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 5 (4), 368-377
- https://doi.org/10.1111/j.1399-0004.1974.tb01708.x
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- A method for rapid prenatal diagnosis of glycogenosis II (Pompe's disease)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1973
- Tissue culture and antenatal detection of molecular diseasesBiochimie, 1972
- Genetic heterogeneity of α‐galactosidase in fabry's diseaseFEBS Letters, 1972
- The Prenatal Diagnosis of Inborn Errors of MetabolismAnnual Review of Medicine, 1972
- Fabry's Disease: Antenatal DetectionScience, 1971
- Genetic Inactivation of the α-Galactosidase Locus in Carriers of Fabry's DiseaseScience, 1970
- Identification ofheterozygous genotype for cystinosis in utero by a new pulse-labeling technique: Preliminary reportThe Journal of Pediatrics, 1970
- Fabry's Disease: Alpha-Galactosidase DeficiencyScience, 1970
- Intrauterine Diagnosis of the Hurler and Hunter SyndromesNew England Journal of Medicine, 1969
- Effects of the Method of Tissue Preparation on the Assay of Tissue Enzyme ActivitiesNature, 1960