Urinary test for identification of Tay-Sachs genotypes
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference8 articles.
1. Tay-Sachs disease: Generalized absence of a β-D-N-acetylexosaminidase compent;Okada;Science,1969
2. Variations of β-N-acetylhexosaminidase pattern in Tay-Sachs disease;Sandhoff;FEBS Letters,1969
3. Identification of Tay-Sachs disease carriers by acrylamide gel electrophoresis;Friedland;Clin. Chim. Acta,1970
4. Detection of Tay-Sachs disease heterozygotes by assay of hexosaminidase A in serum and leukocytes;Y.;J. Pediatr.,1971
5. Tay-Sachs disease: Detection of heterozygotes and homozygotes by serum hexosaminidase assay;O'Brien;N. Engl. J. Med.,1970
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1. Population-based Tay-Sachs screening among Ashkenazi Jewish young adults in the 21st century: Hexosaminidase a enzyme assay is essential for accurate testing;American Journal of Medical Genetics Part A;2009-11
2. Determination of Tay-Sachs genotypes in pregnant women;Clinical Genetics;2008-04-23
3. Iron overload and urinary lysosomal enzyme levels in β-thalassaemia major;European Journal of Pediatrics;1997-07-25
4. Physiological Factors Influencing Enzyme Excretion;Urinary Enzymes;1992
5. Extrarenal Diseases;Urinary Enzymes;1992
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