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- Friedland J., Schneck L., Saifer A., Pourfar M., Volk B. W. Identification of Tay-Sachs disease carriers by acrylamide gel electrophoresis. Clin Chim Acta. 1970 Jun;28(3):397–402. doi: 10.1016/0009-8981(70)90064-1. [DOI] [PubMed] [Google Scholar]
- Navon R., Padeh B. Prenatal diagnosis of Tay-Sachs genotypes. Br Med J. 1971 Oct 2;4(5778):17–20. doi: 10.1136/bmj.4.5778.17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Navon R., Padeh B. Urinary test for identification of Tay-Sachs genotypes. J Pediatr. 1972 Jun;80(6):1026–1030. doi: 10.1016/s0022-3476(72)80020-9. [DOI] [PubMed] [Google Scholar]
- O'Brien J. S., Okada S., Chen A., Fillerup D. L. Tay-sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay. N Engl J Med. 1970 Jul 2;283(1):15–20. doi: 10.1056/NEJM197007022830104. [DOI] [PubMed] [Google Scholar]
- O'Brien J. S., Okada S., Fillerup D. L., Veath M. L., Adornato B., Brenner P. H., Leroy J. G. Tay-Sachs disease: prenatal diagnosis. Science. 1971 Apr 2;172(3978):61–64. doi: 10.1126/science.172.3978.61. [DOI] [PubMed] [Google Scholar]
- Okada S., O'Brien J. S. Tay-Sachs disease: generalized absence of a beta-D-N-acetylhexosaminidase component. Science. 1969 Aug 15;165(3894):698–700. doi: 10.1126/science.165.3894.698. [DOI] [PubMed] [Google Scholar]
- Okada S., Veath M. L., Leroy J., O'Brien J. S. Ganglioside GM2 storage diseases: hexosaminidase deficiencies in cultured fibroblasts. Am J Hum Genet. 1971 Jan;23(1):55–61. [PMC free article] [PubMed] [Google Scholar]
- Okada S., Veath M. L., O'Brien J. S. Juvenile GM2 gangliosidosis: partial deficiency of hexosaminidase A. J Pediatr. 1970 Dec;77(6):1063–1065. doi: 10.1016/s0022-3476(70)80096-8. [DOI] [PubMed] [Google Scholar]
- Padeh B., Navon R. Diagnosis of Tay-Sachs disease by hexosaminidase activity in leukocytes and amniotic fluid cells. Isr J Med Sci. 1971 Feb;7(2):259–263. [PubMed] [Google Scholar]
- Robinson D., Stirling J. L. N-Acetyl-beta-glucosaminidases in human spleen. Biochem J. 1968 Apr;107(3):321–327. doi: 10.1042/bj1070321. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sandhoff K. The hydrolysis of Tay-Sachs ganglioside (TSG) by human N-acetyl-beta-D-hexosaminidase A. FEBS Lett. 1970 Dec 18;11(5):342–344. doi: 10.1016/0014-5793(70)80564-6. [DOI] [PubMed] [Google Scholar]
- Schneck L., Valenti C., Amsterdam D., Friedland J., Adachi M., Volk B. W. Prenatal diagnosis of Tay-Sachs disease. Lancet. 1970 Mar 21;1(7647):582–584. doi: 10.1016/s0140-6736(70)91624-7. [DOI] [PubMed] [Google Scholar]
- Suzuki Y., Berman P. H., Suzuki K. Detection of Tay-Sachs disease heterozygotes by assay of hexosaminidase A in serum and leukocytes. J Pediatr. 1971 Apr;78(4):643–647. doi: 10.1016/s0022-3476(71)80467-5. [DOI] [PubMed] [Google Scholar]