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Journal Abstract Search

114 related items for PubMed ID: 4685842

  • 1. Prenatal diagnosis of trisomy 18. Pathologic findings in 20-week conceptus.
    Hsu LY, Strauss L, Dubin E, Hirschhorn K.
    Am J Dis Child; 1973 Feb; 125(2):290-2. PubMed ID: 4685842
    [No Abstract] [Full Text] [Related]

  • 2. Antenatal diagnosis of fetal abnormality with special reference to amniocentesis.
    Turnbull AC, Gregory PJ, Laurence KM.
    Proc R Soc Med; 1973 Nov; 66(11):1115-8. PubMed ID: 4273030
    [No Abstract] [Full Text] [Related]

  • 3. [Phenocopy of trisomy 18].
    Hongre JF, Toursei F, Staquet MF, Farriaux JP, Walbaum R.
    Ann Pediatr (Paris); 1972 Nov 02; 19(11):825-30. PubMed ID: 4641249
    [No Abstract] [Full Text] [Related]

  • 4. The antenatal diagnosis of trisomy 18.
    Gordon G, Sutherland GR, Bauld R, Bain AD.
    Clin Genet; 1974 Nov 02; 5(2):110-2. PubMed ID: 4829422
    [No Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of double trisomy.
    Hsu LY, Strauss L, Alter AV, Kim HJ, Hirschhorn K.
    Am J Dis Child; 1975 Mar 02; 129(3):381-2. PubMed ID: 123706
    [No Abstract] [Full Text] [Related]

  • 6. [Edwards' syndrome (trisomy 18)].
    Echegaray MA, Scazzola de Bartolomeo B, Iros J, Jacob C.
    Arch Argent Pediatr; 1972 May 02; 70(3):84-8. PubMed ID: 5045485
    [No Abstract] [Full Text] [Related]

  • 7. [Trisomy 21 and trisomy 18 in siblings].
    Girardet P, Grosset L, Juillard E.
    Helv Paediatr Acta; 1972 Dec 02; 27(6):583-9. PubMed ID: 4265243
    [No Abstract] [Full Text] [Related]

  • 8. [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 02; 47(11):808-12. PubMed ID: 23302119
    [Abstract] [Full Text] [Related]

  • 9. Trisomy E with multiple congenital anomalies.
    Biswas B, Heycock JB.
    Br J Clin Pract; 1973 Jul 02; 27(7):269-70. PubMed ID: 4727309
    [No Abstract] [Full Text] [Related]

  • 10. [Case of double aneuploidy: trisomy 18 and XXY].
    Bach C, Toublanc JE, Gautier M.
    Ann Genet; 1973 Mar 02; 16(1):61-6. PubMed ID: 4541812
    [No Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of E trisomy syndrome by fetography.
    Ogita S, Hasegawa H, Matsumoto M, Kamei T, Shimamoto T.
    Obstet Gynecol; 1974 Jun 02; 43(6):887-92. PubMed ID: 4597791
    [No Abstract] [Full Text] [Related]

  • 12. [Edward's syndrome in a newborn].
    Wiśniewski L, Gawrońska H, Lech H.
    Pediatr Pol; 1973 Jul 02; 48(7):881-5. PubMed ID: 4738455
    [No Abstract] [Full Text] [Related]

  • 13. Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.
    Müller H, Bühler EM, Signer E, Egli F, Stalder GR.
    J Med Genet; 1972 Dec 02; 9(4):462-7. PubMed ID: 4646556
    [No Abstract] [Full Text] [Related]

  • 14. [Edwards syndrome (E-ltrisomy)].
    Otgon M, Mukhin IuK.
    Akush Ginekol (Mosk); 1972 Mar 02; 48(3):71-2. PubMed ID: 5011385
    [No Abstract] [Full Text] [Related]

  • 15. The clinical and genetic picture of trisomy 18 (Edwards' syndrome).
    Shibata K, Waldenmaier C, Hirsch W.
    Z Kinderheilkd; 1973 Dec 12; 116(1):13-22. PubMed ID: 4129502
    [No Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of craniomaxillofacial malformations: a characterization of phenotypes in trisomies 13, 18, and 21 by ultrasound and pathology.
    Ettema AM, Wenghoefer M, Hansmann M, Carels CE, Borstlap WA, Bergé SJ.
    Cleft Palate Craniofac J; 2010 Mar 12; 47(2):189-96. PubMed ID: 19860526
    [Abstract] [Full Text] [Related]

  • 17. Long survival in a male with 18-trisomy syndrome and Wilms' tumor.
    Geiser CF, Schindler AM.
    Pediatrics; 1969 Jul 12; 44(1):111-6. PubMed ID: 4307567
    [No Abstract] [Full Text] [Related]

  • 18. Trends in timing of prenatal diagnosis and abortion for fetal chromosomal abnormalities.
    Hume H, Chasen ST.
    Am J Obstet Gynecol; 2015 Oct 12; 213(4):545.e1-4. PubMed ID: 26070711
    [Abstract] [Full Text] [Related]

  • 19. [Phenotype and karyologic aspects of Edwards' syndrome (case report)].
    Piazzi G, Salvioli GP.
    Clin Pediatr (Bologna); 1969 Mar 12; 51(3):117-30. PubMed ID: 5405112
    [No Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis of nonmosaic trisomy 9 and related ultrasound findings at 11.7 weeks.
    Pinette MG, Pan Y, Chard R, Pinette SG, Blackstone J.
    J Matern Fetal Med; 1998 Mar 12; 7(1):48-50. PubMed ID: 9502671
    [Abstract] [Full Text] [Related]

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