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10. Distribution of three alpha-chain beta-hexosaminidase A mutations among Tay-Sachs carriers. Grebner EE, Tomczak J. Am J Hum Genet; 1991 Mar 05; 48(3):604-7. PubMed ID: 1825595 [Abstract] [Full Text] [Related]
11. Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis. Frisch A, Colombo R, Michaelovsky E, Karpati M, Goldman B, Peleg L. Hum Genet; 2004 Mar 05; 114(4):366-76. PubMed ID: 14727180 [Abstract] [Full Text] [Related]
12. Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs disease. Akerman BR, Natowicz MR, Kaback MM, Loyer M, Campeau E, Gravel RA. Am J Hum Genet; 1997 May 05; 60(5):1099-106. PubMed ID: 9150157 [Abstract] [Full Text] [Related]
13. Pedigree discriminant analysis of two French Canadian Tay-Sachs families. Keats BJ, Elston RC, Andermann E. Genet Epidemiol; 1987 May 05; 4(2):77-85. PubMed ID: 2953646 [Abstract] [Full Text] [Related]
18. A gel electrophoretic assay for detecting the insertion defect in Ashkenazi Jewish carriers of Tay-Sachs disease. Shore S, Myerowitz R. Anal Biochem; 1990 Apr 05; 186(1):179-81. PubMed ID: 2356966 [Abstract] [Full Text] [Related]
20. Comparison of enzyme and DNA analysis in a Tay-Sachs disease carrier screening program. Yoo HW, Astrin KH, Desnick RJ. J Korean Med Sci; 1993 Feb 05; 8(1):84-91. PubMed ID: 8343225 [Abstract] [Full Text] [Related] Page: [Next] [New Search]