A method for rapid prenatal diagnosis of glycogenosis II (Pompe's disease)
- 1 December 1973
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 49 (3) , 361-375
- https://doi.org/10.1016/0009-8981(73)90234-9
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Acid α-glucosidase in amniotic fluidBiochemical Medicine, 1973
- A scanning device for the double beam leitz interference microscopeHistochemistry and Cell Biology, 1973
- Tissue culture and antenatal detection of molecular diseasesBiochimie, 1972
- Alpha-1,4 glucosidase activity in Pompe's diseaseThe Journal of Pediatrics, 1971
- Prenatal Genetic DiagnosisNew England Journal of Medicine, 1970
- IN-UTERO DETECTION OF POMPE'S DISEASEThe Lancet, 1970
- IN-UTERO DETECTION OF TYPE-II GLYCOGENOSIS (POMPE'S DISEASE)The Lancet, 1969
- Type II GlycogenosisAmerican Journal of Diseases of Children, 1966
- α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)Biochemical Journal, 1963
- THE QUANTITATIVE HISTOCHEMISTRY OF THE BRAINJournal of Histochemistry & Cytochemistry, 1953