Prenatal diagnosis of galactosemia
- 1 February 1977
- journal article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 74 (3) , 227-235
- https://doi.org/10.1016/0009-8981(77)90289-3
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
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- Galactose-1-phosphate uridyltransferase and galactokinase activity in cultured human diploid fibroblasts and peripheral blood leukocytesJournal of Clinical Investigation, 1969
- Estimation of galactose-1-phosphate in erythrocytes: A rapid and simple enzymatic methodClinica Chimica Acta; International Journal of Clinical Chemistry, 1969
- An improved electrophoretic procedure for galactose-l-phosphate uridyl transferase: Demonstration of multiple activity bands with the duarte variantBiochemical and Biophysical Research Communications, 1969
- An improved procedure for the assay of hemolysate galactose-1-phosphate uridyl transferase activity by the use of 14C-labeled galactose-1-phosphateClinica Chimica Acta; International Journal of Clinical Chemistry, 1967
- Hereditary Galactokinase Deficiency, a Newly Recognized Cause of Juvenile Cataracts31Pediatric Research, 1966
- Quantitative analysis of serum and urine sugars by gas chromatographyClinica Chimica Acta; International Journal of Clinical Chemistry, 1964
- STUDIES ON CELL LINES DEVELOPED FROM THE TISSUES OF PATIENTS WITH GALACTOSEMIAThe Journal of Experimental Medicine, 1961
- The Value of Galactose Phosphate Determinations in the treatment of GalactosaemiaArchives of Disease in Childhood, 1960
- Galactosemia, a congenital defect in a nucleotide transferaseBiochimica et Biophysica Acta, 1956