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PUBMED FOR HANDHELDS

Journal Abstract Search


126 related items for PubMed ID: 153444

  • 1. Prenatal diagnosis in New South Wales: comparative view of the first 1000 cases of chromosomal, sex-linked, and metabolic referrals.
    Daniel A, Lam-Po-Tang PR.
    Med J Aust; 1978 Oct 07; 2(8):352-7. PubMed ID: 153444
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis in 3,000 women for chromosome, X-linked, and metabolic disorders.
    Daniel A, Stewart L, Saville T, Brookwell R, Paull H, Purvis-Smith S, Lam-Po-Tang PR.
    Am J Med Genet; 1982 Jan 07; 11(1):61-75. PubMed ID: 7065004
    [Abstract] [Full Text] [Related]

  • 3. European experience with prenatal diagnosis of congenital disease: a survey of 6121 cases.
    Galjaard H.
    Cytogenet Cell Genet; 1976 Jan 07; 16(6):453-67. PubMed ID: 789015
    [Abstract] [Full Text] [Related]

  • 4. [Prenatal diagnosis in 350 amniocenteses].
    Grether P, Zavaleta MJ, de la Luna E, Sánchez-Solis V, Hernández C, Karchmer S.
    Ginecol Obstet Mex; 1991 Nov 07; 59():317-22. PubMed ID: 1797616
    [Abstract] [Full Text] [Related]

  • 5. Chromosomal abnormality rates at amniocentesis and in live-born infants.
    Hook EB, Cross PK, Schreinemachers DM.
    JAMA; 1983 Apr 15; 249(15):2034-8. PubMed ID: 6220164
    [Abstract] [Full Text] [Related]

  • 6. Age-specific incidences of chromosome abnormalities at the second trimester amniocentesis for Japanese mothers aged 35 and older: collaborative study of 5484 cases.
    Yaegashi N, Senoo M, Uehara S, Suzuki H, Maeda T, Fujimori K, Hirahara F, Yajima A.
    J Hum Genet; 1998 Apr 15; 43(2):85-90. PubMed ID: 9621511
    [Abstract] [Full Text] [Related]

  • 7. [Prenatal diagnosis. Review, personal and prospective studies].
    Engel E, Empson J, DeLozier D, McGee B, da Costa Woodson E, Engel-de Montmollin M, Carter T, Lorber C, Cassidy SB, Millis J, Heller RM, Boehm F, Vanhooydonk J.
    Schweiz Med Wochenschr; 1979 Jul 07; 109(27):998-1010. PubMed ID: 88763
    [Abstract] [Full Text] [Related]

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  • 9. Prenatal cytogenetic analysis of women with high risk for genetic disorders.
    Rary JM, Park IJ, Heller RH, Jones HW, Baramki TA.
    J Hered; 1974 Jul 07; 65(4):209-12. PubMed ID: 4278231
    [Abstract] [Full Text] [Related]

  • 10. Prenatal genetic diagnosis in 350 amniocenteses.
    Crandall BF, Lebherz TB.
    Obstet Gynecol; 1976 Aug 07; 48(2):158-62. PubMed ID: 133307
    [Abstract] [Full Text] [Related]

  • 11. [Value of detection of cell-free fetal DNA in maternal plasma in the prenatal diagnosis of chromosomal abnormalities].
    Wang SJ, Gao ZY, Lu YP, Li YL, You YQ, Zhang LW, Wang LX, Xu H.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Nov 07; 47(11):808-12. PubMed ID: 23302119
    [Abstract] [Full Text] [Related]

  • 12. Genetics, amniocentesis, and abortion.
    Hirschhorn K.
    Mt Sinai J Med; 1984 Nov 07; 51(1):15-7. PubMed ID: 6608672
    [Abstract] [Full Text] [Related]

  • 13. Amniocentesis for antenatal diagnosis.
    Elias S.
    Compr Ther; 1982 Jun 07; 8(6):21-5. PubMed ID: 6179702
    [Abstract] [Full Text] [Related]

  • 14. Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration. A European Collaborative Study on Prenatal Diagnoses 1981.
    Stene J, Stene E, Mikkelsen M.
    Prenat Diagn; 1984 Jun 07; 4 Spec No():81-95. PubMed ID: 6235486
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  • 15.
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  • 16. Prenatal diagnosis of chromosomal abnormalities: analysis of 1000 consecutive amniotic fluids.
    Bell JA, Ansford AJ.
    Aust N Z J Obstet Gynaecol; 1981 Nov 07; 21(4):207-10. PubMed ID: 6462129
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  • 18. Screening for fetal chromosome aberrations in early pregnancy.
    Ferguson-Smith MA, Ferguson-Smith ME.
    J Clin Pathol Suppl (R Coll Pathol); 1976 Nov 07; 10():165-76. PubMed ID: 135003
    [Abstract] [Full Text] [Related]

  • 19. The antenatal detection of genetic disorders. Current status and future prospects.
    Golbus MS.
    Obstet Gynecol; 1976 Oct 07; 48(4):497-506. PubMed ID: 135214
    [No Abstract] [Full Text] [Related]

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