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Journal Abstract Search

190 related items for PubMed ID: 7484451

  • 1. The origin of numerical chromosome abnormalities.
    Jacobs PA, Hassold TJ.
    Adv Genet; 1995; 33():101-33. PubMed ID: 7484451
    [No Abstract] [Full Text] [Related]

  • 2. Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses.
    Ferguson-Smith MA, Yates JR.
    Prenat Diagn; 1984; 4 Spec No():5-44. PubMed ID: 6235485
    [No Abstract] [Full Text] [Related]

  • 3. Cytogenetics of pregnancy wastage.
    Boué A, Boué J, Gropp A.
    Adv Hum Genet; 1985; 14():1-57. PubMed ID: 3887861
    [No Abstract] [Full Text] [Related]

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  • 5. Trisomy in man.
    Hassold TJ, Jacobs PA.
    Annu Rev Genet; 1984; 18():69-97. PubMed ID: 6241455
    [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; 43(2):85-90. PubMed ID: 9621511
    [Abstract] [Full Text] [Related]

  • 7. Antenatal diagnosis of chromosomal disorders.
    Simpson JL.
    Clin Obstet Gynaecol; 1980 Apr; 7(1):13-26. PubMed ID: 6445807
    [No Abstract] [Full Text] [Related]

  • 8. Chromosome aberrations in 2159 consecutive newborn babies.
    Sergovich F, Valentine GH, Chen AT, Kinch RA, Smout MS.
    N Engl J Med; 1969 Apr 17; 280(16):851-5. PubMed ID: 4238063
    [No Abstract] [Full Text] [Related]

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  • 10. The potential usefulness of computerized chromosome analysis in human genetics.
    Hsu LY, Hirschhorn K.
    Comput Biol Med; 1972 Oct 17; 2(2):99-106. PubMed ID: 4274148
    [No Abstract] [Full Text] [Related]

  • 11. Human aneuploidy: incidence, origin, and etiology.
    Hassold T, Abruzzo M, Adkins K, Griffin D, Merrill M, Millie E, Saker D, Shen J, Zaragoza M.
    Environ Mol Mutagen; 1996 Oct 17; 28(3):167-75. PubMed ID: 8908177
    [No Abstract] [Full Text] [Related]

  • 12. [Incidence of chromosome anomalies in newborn infants].
    Wagenbichler P, Golob E.
    Gynakol Rundsch; 1975 Oct 17; 15(3):225-39. PubMed ID: 131056
    [No Abstract] [Full Text] [Related]

  • 13. A cytogenetic survey of 11,680 newborn infants.
    Jacobs PA, Melville M, Ratcliffe S, Keay AJ, Syme J.
    Ann Hum Genet; 1974 May 17; 37(4):359-76. PubMed ID: 4277977
    [No Abstract] [Full Text] [Related]

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  • 16. Chromosome studies in 5,049 consecutive newborn children.
    Friedrich U, Nielsen J.
    Clin Genet; 1973 May 17; 4(4):333-43. PubMed ID: 4747810
    [No Abstract] [Full Text] [Related]

  • 17. Banding analysis of abnormal karyotypes in spontaneous abortion.
    Kajii T, Oama K, Niikawa N, Ferrier A, Avirachan S.
    Am J Hum Genet; 1973 Sep 17; 25(5):539-47. PubMed ID: 4741848
    [No Abstract] [Full Text] [Related]

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  • 19. Frequency of chromosomal abnormalities in miscarriages and perinatal deaths.
    Alberman ED, Creasy MR.
    J Med Genet; 1977 Oct 17; 14(5):313-5. PubMed ID: 563464
    [No Abstract] [Full Text] [Related]

  • 20. Chromosome anomalies of infants dying during the perinatal period and premature newborn.
    Kuleshov NP.
    Hum Genet; 1976 Feb 29; 31(2):151-60. PubMed ID: 129431
    [Abstract] [Full Text] [Related]

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