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8. Tay-Sachs disease screening and diagnosis: evolving technologies. Hechtman P; Kaplan F DNA Cell Biol; 1993 Oct; 12(8):651-65. PubMed ID: 8397824 [TBL] [Abstract][Full Text] [Related]
9. Primer system for single cell detection of double mutation for Tay-Sachs disease. Liu MC; Drury KC; Kipersztok S; Zheng W; Williams RS J Assist Reprod Genet; 2000 Feb; 17(2):121-6. PubMed ID: 10806593 [TBL] [Abstract][Full Text] [Related]
10. Screening for reproductive counseling: social, ethical, and medicolegal issues in the Tay-Sachs disease experience. Kaback MM Prog Clin Biol Res; 1982; 103 Pt B():447-59. PubMed ID: 7163239 [No Abstract] [Full Text] [Related]
11. Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene. Myerowitz R Hum Mutat; 1997; 9(3):195-208. PubMed ID: 9090523 [TBL] [Abstract][Full Text] [Related]
12. Ethical Issues with Genetic Testing for Tay-Sachs. Clayton T J Christ Nurs; 2017; 34(4):246-249. PubMed ID: 28902054 [TBL] [Abstract][Full Text] [Related]
14. Heterozygote advantage in Tay-Sachs carriers? Spyropoulos B; Moens PB; Davidson J; Lowden JA Am J Hum Genet; 1981 May; 33(3):375-80. PubMed ID: 7246543 [TBL] [Abstract][Full Text] [Related]
15. ACOG committee opinion. Number 318, October 2005. Screening for Tay-Sachs disease. ACOG Committee on Genetics Obstet Gynecol; 2005 Oct; 106(4):893-4. PubMed ID: 16199656 [TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of Tay-Sachs disease. Ambani LM; Bhatia RS; Shah SB; Apte BN Indian Pediatr; 1989 Oct; 26(10):1052-3. PubMed ID: 2630450 [No Abstract] [Full Text] [Related]
17. Control of hereditary disorders. Porter IH Annu Rev Public Health; 1982; 3():277-319. PubMed ID: 6756430 [No Abstract] [Full Text] [Related]
18. Tay-Sachs disease--carrier screening, prenatal diagnosis, and the molecular era. An international perspective, 1970 to 1993. The International TSD Data Collection Network. Kaback M; Lim-Steele J; Dabholkar D; Brown D; Levy N; Zeiger K JAMA; 1993 Nov; 270(19):2307-15. PubMed ID: 8230592 [TBL] [Abstract][Full Text] [Related]
19. Diagnostic heteroduplexes: simple detection of carriers of a 4-bp insertion mutation in Tay-Sachs disease. Triggs-Raine BL; Gravel RA Am J Hum Genet; 1990 Jan; 46(1):183-4. PubMed ID: 2294750 [No Abstract] [Full Text] [Related]
20. Carrier screening for cystic fibrosis, Gaucher disease, and Tay-Sachs disease in the Ashkenazi Jewish population: the first 1000 cases at New York University Medical Center, New York, NY. Kronn D; Jansen V; Ostrer H Arch Intern Med; 1998 Apr; 158(7):777-81. PubMed ID: 9554684 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]