Tay-Sachs disease heterozygote detection: use of a centrifugal analyser for automation of hexosaminidase assays with two different artificial substrates.-Reference-Cited by-同舟云学术

Tay-Sachs disease heterozygote detection: use of a centrifugal analyser for automation of hexosaminidase assays with two different artificial substrates.

Published:1991-02-01 Issue:2 Volume:28 Page:101-109
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Landels E C,Ellis I H,Bobrow M,Fensom A H

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. The GM2 gangliosidoses;Sandhoff, K.; Conzelmann, E.; Neufeld, E.F.; Kaback, M.M.; Suzuki, K.,1989

2. Tay-Sachs disease: detection of heterozygotes and homozygotes by serum hexosaminidase assay;O'Brien, J.S.; Okada, S.; Chen, A.; Fillerup, D.L.;N EnglJ3 Med,1970

3. Heterozygote detection in Tay-Sachs disease: a prototype community screening programme for the prevention of recessive genetic disorders;Kaback, M.M.; Zeiger, R.S.;Adv Exp Biol Med,1972

4. Automated thermal fractionation of serum hexosaminidase: effect of alteration in reaction variables and implication for Tay-Sachs heterozygote screening;Kaback, M.M.; Bailin, G.; Hirsch, P.; Roy, C.,1977

5. Separation and characterisation of N-acetyl-fl-glucosaminidases A and P from maternal serum;Stirling, J.L.;Biochim Biophys Acta,1972

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