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Journal Abstract Search

96 related items for PubMed ID: 2954695

  • 21. Prenatal diagnosis of Tay-Sachs disease.
    Dreyfus JC, Poenaru L.
    Lancet; 1979 Jun 16; 1(8129):1296. PubMed ID: 87758
    [No Abstract] [Full Text] [Related]

  • 22. Opinion exchange: is it better to know the worst?
    RN; 1982 Mar 16; 45(3):48-9, 124. PubMed ID: 6918093
    [No Abstract] [Full Text] [Related]

  • 23. Prenatal diagnosis of tay-sachs b1 variant in a maharashtrian family.
    Sheth J, Bhattacharya R, Sheth F.
    Indian Pediatr; 2002 Jul 16; 39(7):704-6. PubMed ID: 12147910
    [No Abstract] [Full Text] [Related]

  • 24. Will prenatal diagnosis with selective abortion affect society's attitude toward the handicapped?
    Motulsky AG, Murray J.
    Prog Clin Biol Res; 1983 Jul 16; 128():277-91. PubMed ID: 6227010
    [No Abstract] [Full Text] [Related]

  • 25. Maternal serum hexosaminidase A in pregnancy: effects of gestational age and fetal genotype.
    Ben-Yoseph Y, Pack BA, Thomas PM, Nadler HL, Kaback MM.
    Am J Med Genet; 1988 Apr 16; 29(4):891-9. PubMed ID: 2969680
    [Abstract] [Full Text] [Related]

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  • 28. Morphology of the placenta in fetal I-cell disease.
    Rapola J, Aula P.
    Clin Genet; 1977 Feb 16; 11(2):107-13. PubMed ID: 837559
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  • 30. [Prenatal biochemical diagnosis of Tay-Sachs disease].
    Rozenfel'd EL, Tsvetkova IV, Kozina AB, Rozovskiĭ IS, Kovrigina NG.
    Vopr Med Khim; 1972 Feb 16; 18(4):445-6. PubMed ID: 4661856
    [No Abstract] [Full Text] [Related]

  • 31. [Hydrops fetalis as an indication for a systematic investigation into the presence of lysosomal storage diseases].
    Janssens PM, de Groot AN, de Jong JG, Liebrand-van Sambeek ML, Smits A, Wevers RA.
    Ned Tijdschr Geneeskd; 2004 Feb 07; 148(6):264-8. PubMed ID: 15004952
    [Abstract] [Full Text] [Related]

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  • 33. [Tay-Sachs disease: prenatal detection and diagnosis].
    Delvin EE, Scriver CR, Pottier A, Clow CL, Goldman H.
    Union Med Can; 1972 Apr 07; 101(4):683-8. PubMed ID: 5062350
    [No Abstract] [Full Text] [Related]

  • 34. A modified method for prenatal diagnosis of Tay-Sachs disease in cell-free amniotic fluid.
    Navon R, Wiselter J, Modan M.
    Monogr Hum Genet; 1978 Apr 07; 9():186-92. PubMed ID: 732839
    [No Abstract] [Full Text] [Related]

  • 35. Prenatal diagnosis of neurolipidoses.
    Grebner EE, Jackson LG.
    Ann Clin Lab Sci; 1982 Apr 07; 12(5):381-7. PubMed ID: 6215890
    [Abstract] [Full Text] [Related]

  • 36. Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases.
    Ramsay SL, Maire I, Bindloss C, Fuller M, Whitfield PD, Piraud M, Hopwood JJ, Meikle PJ.
    Mol Genet Metab; 2004 Nov 07; 83(3):231-8. PubMed ID: 15542394
    [Abstract] [Full Text] [Related]

  • 37. Factors affecting performance of prenatal genetic testing by Israeli Jewish women.
    Sher C, Romano-Zelekha O, Green MS, Shohat T.
    Am J Med Genet A; 2003 Jul 30; 120A(3):418-22. PubMed ID: 12838566
    [Abstract] [Full Text] [Related]

  • 38. Detection of chromosome aberrations during prenatal genetic testing for single gene disorders.
    Chen CP, Lin SP.
    Prenat Diagn; 2004 Nov 30; 24(11):924-5. PubMed ID: 15565556
    [No Abstract] [Full Text] [Related]

  • 39. Prenatal diagnosis of a Japanese family at risk for Tay-Sachs disease. Application of a fluorescent competitive allele-specific polymerase chain reaction (PCR) method.
    Tamasu S, Nishio H, Ayaki H, Lee MJ, Mizutori M, Takeshima Y, Nakamura H, Matsuo M, Maruo T, Sumino K.
    Kobe J Med Sci; 1999 Dec 30; 45(6):259-70. PubMed ID: 10985159
    [Abstract] [Full Text] [Related]

  • 40. Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene.
    Myerowitz R.
    Hum Mutat; 1997 Dec 30; 9(3):195-208. PubMed ID: 9090523
    [Abstract] [Full Text] [Related]

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