These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

105 related articles for article (PubMed ID: 1973519)

  • 1. Carrier screening for Tay-Sachs disease.
    Scriver CR; Clow CL
    Lancet; 1990 Jul; 336(8708):191. PubMed ID: 1973519
    [No Abstract]   [Full Text] [Related]  

  • 2. Polymerase chain reaction-generated heteroduplexes from Ashkenazi Tay-Sachs carriers with an insertion mutation can be detected on agarose gels.
    Shore S; Myerowitz R
    Am J Hum Genet; 1990 Jul; 47(1):169. PubMed ID: 2349947
    [No Abstract]   [Full Text] [Related]  

  • 3. Picture of the month. Tay-Sachs disease.
    Arisoy AE; Ozden S; Arisoy ES; Kocabay K; Guvenc H; Tunnessen WW
    Am J Dis Child; 1992 Jun; 146(6):767-8. PubMed ID: 1534438
    [No Abstract]   [Full Text] [Related]  

  • 4. Carrier screening for Tay-Sachs disease.
    Scriver CR; Clow CL
    Lancet; 1990 Apr; 335(8693):856. PubMed ID: 1969578
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. The Dor Yeshorim story: community-based carrier screening for Tay-Sachs disease.
    Ekstein J; Katzenstein H
    Adv Genet; 2001; 44():297-310. PubMed ID: 11596991
    [No Abstract]   [Full Text] [Related]  

  • 7. Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.
    Hussein N; Weng SF; Kai J; Kleijnen J; Qureshi N
    Cochrane Database Syst Rev; 2015 Aug; 2015(8):CD010849. PubMed ID: 26264938
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tay-Sachs disease heterozygote detection: use of a centrifugal analyser for automation of hexosaminidase assays with two different artificial substrates.
    Landels EC; Ellis IH; Bobrow M; Fensom AH
    J Med Genet; 1991 Feb; 28(2):101-9. PubMed ID: 1825851
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Screening for the Tay-Sachs carrier: a compromise program.
    Potter JL; Robinson HB
    Clin Chem; 1981 Apr; 27(4):523-5. PubMed ID: 7471417
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal exclusion of Tay-Sachs disease by DNA analysis.
    Triggs-Raine BL; Archibald A; Gravel RA; Clarke JT
    Lancet; 1990 May; 335(8698):1164. PubMed ID: 1971898
    [No Abstract]   [Full Text] [Related]  

  • 12. Tay Sachs disease carrier screening in schools: educational alternatives and cheekbrush sampling.
    Gason AA; Metcalfe SA; Delatycki MB; Petrou V; Sheffield E; Bankier A; Aitken M
    Genet Med; 2005; 7(9):626-32. PubMed ID: 16301864
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multimedia messages in genetics: design, development, and evaluation of a computer-based instructional resource for secondary school students in a Tay Sachs disease carrier screening program.
    Gason AA; Aitken M; Delatycki MB; Sheffield E; Metcalfe SA
    Genet Med; 2004; 6(4):226-31. PubMed ID: 15266211
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tay-Sachs disease: psychologic care of carriers and affected families.
    Schweitzer-Miller L
    Adv Genet; 2001; 44():341-7. PubMed ID: 11596995
    [No Abstract]   [Full Text] [Related]  

  • 15. A genetic screening programme for Tay-Sachs disease and cystic fibrosis for Australian Jewish high school students.
    Barlow-Stewart K; Burnett L; Proos A; Howell V; Huq F; Lazarus R; Aizenberg H
    J Med Genet; 2003 Apr; 40(4):e45. PubMed ID: 12676918
    [No Abstract]   [Full Text] [Related]  

  • 16. One worked; the other didn't.
    Roberts L
    Science; 1990 Jan; 247(4938):18. PubMed ID: 2294586
    [No Abstract]   [Full Text] [Related]  

  • 17. The incidence and carrier frequency of Tay-Sachs disease in the French-Canadian population of Quebec based on retrospective data from 24 years, 1992-2015.
    Sillon G; Allard P; Drury S; Rivière JB; De Bie I
    J Genet Couns; 2020 Dec; 29(6):1173-1185. PubMed ID: 32302469
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tay-Sachs disease carrier screening: a 21-year experience.
    D'Souza G; McCann CL; Hedrick J; Fairley C; Nagel HL; Kushner JD; Kessel R
    Genet Test; 2000; 4(3):257-63. PubMed ID: 11142756
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cost-effectiveness of a school-based Tay-Sachs and cystic fibrosis genetic carrier screening program.
    Warren E; Anderson R; Proos AL; Burnett LB; Barlow-Stewart K; Hall J
    Genet Med; 2005 Sep; 7(7):484-94. PubMed ID: 16170240
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Population-specific screening by mutation analysis for diseases frequent in Ashkenazi Jews.
    DeMarchi JM; Caskey CT; Richards CS
    Hum Mutat; 1996; 8(2):116-25. PubMed ID: 8844209
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.