Determination of Tay-Sachs genotypes in pregnant women
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1973.tb01158.x/fullpdf
Reference6 articles.
1. Identification of Tay-Sachs disease carriers by acrylamide gel electrophoresis;Friedland;Clin. chim. Acta,1970
2. Urinary test for identification of Tay-Sachs genotypes;Navon;J. Pediat.,1972
3. Tay-Sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay;O'Brien;New Engl. J. Med.,1970
4. Tay-Sachs disease: Generalized absence of a B-D-N-acetylhexosaminidase component;Okada;Science,1969
5. Diagnosis of Tay-Sachs disease by hexosaminidase activity in leukocytes and amniotic fluid cells;Padeh;Israel J. med. Sci.,1971
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