First Trimester Diagnosis of Glycogen Storage Disease Type II and Type III
- 1 April 1989
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 12 (S2) , 289-291
- https://doi.org/10.1007/bf03335401
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- First trimester diagnosis of Pompe's disease (glycogenosis type II) with normal outcome: assay of acid α-glucosidase in chorionic villous biopsy using antibodiesClinical Genetics, 1986
- Diagnosis of Pompe's disease using leukocyte preparations. Kinetic and immunological studies of 1,4-α-glucosidase in human fetal and adult tissues and cultured cellsClinica Chimica Acta; International Journal of Clinical Chemistry, 1985
- A simple assay for amylo-1,6-glucosidase to detect heterozygotes for glycogenosis type III in erythrocytes.Clinical Chemistry, 1984