PRENATAL DIAGNOSIS OF TWO HURLER FETUSES USING AN IMPROVED ASSAY FOR METHYLUMBELLIFERYL-α-L-IDURONEDASE
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference9 articles.
1. Fluorimetric assay for prenatal detection of Hurler and Scheie homozygotes or heterozygotes;Stirling;Lancet,1978
2. α-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells;Hall;Arch Biochem. Biophys,1973
3. Genetic errors of mucopolysaccharide degradation;Bach;Biochem Soc Trans,1973
4. A fluorimetric assay using 4-methylumbelliferyl α-L-iduronide for estimation of α-iduronidase activity and the detection of Hurler and Scheie syndromes;Hopwood;Clin Chim Acta,1979
5. α-L-iduronidase in lysosomal extracts;Weissman;Biochem Biophys Res Commun,1972
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2. Determination of Biological Variance and Validation of a Fluorometric Assay for Measurement of α-l-Iduronidase Activity in Dried Blood Spots Samples: The First Experience in Iran;Indian Journal of Clinical Biochemistry;2014-07-30
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5. Recent advances in the prenatal diagnosis of the mucopolysaccharidoses;Prenatal Diagnosis;1994-01
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