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 *

68 related articles for article (PubMed ID: 6377528)

  • 1. Tay-Sachs disease and the persistence of lethal autosomal recessive genes in human populations.
    Koeslag JH; Schach SR; Melzer CW
    S Afr Med J; 1984 Jul; 66(3):87-9. PubMed ID: 6377528
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Tay-Sachs disease and the role of reproductive compensation in the maintenance of ethnic variations in the incidence of autosomal recessive disease.
    Koeslag JH; Schach SR
    Ann Hum Genet; 1984 Jul; 48(3):275-81. PubMed ID: 6465844
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tay-Sachs disease in persons of French-Canadian heritage in northern New England.
    Palomaki GE; Williams J; Haddow JE; Natowicz MR
    Am J Med Genet; 1995 May; 56(4):409-12. PubMed ID: 7604851
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Social mechanisms in the population genetics of Tay-Sachs and other lethal autosomal recessive diseases: a computer simulation model.
    McKusick KB; Schach SR; Koeslag JH
    Am J Med Genet; 1990 Jun; 36(2):178-82. PubMed ID: 2368806
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. On the perpetuation of relic genes having an inviable homozygote.
    Koeslag JH; Schach SR
    Ann Hum Genet; 1985 Oct; 49(4):291-302. PubMed ID: 4073837
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Biochemical, molecular and social aspects of carrier screening for Tay-Sachs disease].
    Peleg L; Gazit E; Goldman B; Akstein E
    Harefuah; 1995 Dec; 129(11):475-80. PubMed ID: 8846957
    [No Abstract]   [Full Text] [Related]  

  • 8. Molecular epidemiology of Tay-Sachs disease.
    Risch N
    Adv Genet; 2001; 44():233-52. PubMed ID: 11596986
    [No Abstract]   [Full Text] [Related]  

  • 9. Carrier parents of Tay Sachs disease and beta-thalassemia.
    Shah B; Bhavsar R
    Indian Pediatr; 2005 May; 42(5):498-9. PubMed ID: 15923705
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Screening for carriers of Tay-Sachs disease among Ashkenazi Jews. A comparison of DNA-based and enzyme-based tests.
    Triggs-Raine BL; Feigenbaum AS; Natowicz M; Skomorowski MA; Schuster SM; Clarke JT; Mahuran DJ; Kolodny EH; Gravel RA
    N Engl J Med; 1990 Jul; 323(1):6-12. PubMed ID: 2355960
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of an altered splice site in Ashkenazi Tay-Sachs disease.
    Arpaia E; Dumbrille-Ross A; Maler T; Neote K; Tropak M; Troxel C; Stirling JL; Pitts JS; Bapat B; Lamhonwah AM
    Nature; 1988 May; 333(6168):85-6. PubMed ID: 3362213
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GM2 gangliosidoses in Spain: analysis of the HEXA and HEXB genes in 34 Tay-Sachs and 14 Sandhoff patients.
    Gort L; de Olano N; Macías-Vidal J; Coll MA;
    Gene; 2012 Sep; 506(1):25-30. PubMed ID: 22789865
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening for genetic disorders among Jews: how should the Tay-Sachs screening program be continued?
    Zlotogora J; Leventhal A
    Isr Med Assoc J; 2000 Sep; 2(9):665-7. PubMed ID: 11062764
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Late onset Tay-Sachs disease in mice with targeted disruption of the Hexa gene: behavioral changes and pathology of the central nervous system.
    Miklyaeva EI; Dong W; Bureau A; Fattahie R; Xu Y; Su M; Fick GH; Huang JQ; Igdoura S; Hanai N; Gravel RA
    Brain Res; 2004 Mar; 1001(1-2):37-50. PubMed ID: 14972652
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tay-Sachs disease as a model for screening inborn errors.
    Blitzer MG; McDowell GA
    Clin Lab Med; 1992 Sep; 12(3):463-80. PubMed ID: 1355703
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pedigree discriminant analysis of two French Canadian Tay-Sachs families.
    Keats BJ; Elston RC; Andermann E
    Genet Epidemiol; 1987; 4(2):77-85. PubMed ID: 2953646
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
    Guetta E; Peleg L
    Methods Mol Biol; 2008; 444():147-59. PubMed ID: 18425478
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Tay-Sachs disease].
    Tanaka A
    Nihon Rinsho; 1993 Sep; 51(9):2281-5. PubMed ID: 8411703
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carrier screening for Tay-Sachs.
    Ellis I
    Nursing (Lond); 1991 Sep 12-25; 4(41):16-8. PubMed ID: 1945106
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.