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Journal Abstract Search

376 related items for PubMed ID: 10719324

  • 21. Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term culture.
    Wegner RD, Schröck E, Obladen M, Becker R, Stumm M, Sperling K.
    Prenat Diagn; 1996 Aug; 16(8):741-8. PubMed ID: 8878285
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  • 23. Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis.
    Calabrese G, Baldi M, Fantasia D, Sessa MT, Kalantar M, Holzhauer C, Alunni-Fabbroni M, Palka G, Sitar G.
    Clin Genet; 2012 Aug; 82(2):131-9. PubMed ID: 21895636
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  • 25. [Clinical approach to prenatal diagnosis of chromosome abnormalities].
    Herlicoviez M.
    Reprod Nutr Dev; 1990 Aug; Suppl 1():139s-145s. PubMed ID: 2206291
    [Abstract] [Full Text] [Related]

  • 26. Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis.
    Prontera P, Buldrini B, Aiello V, Gruppioni R, Bonfatti A, Venti G, Ferlini A, Sensi A, Calzolari E, Donti E.
    Prenat Diagn; 2006 Jun; 26(6):571-6. PubMed ID: 16683276
    [Abstract] [Full Text] [Related]

  • 27. Prenatal diagnosis of Prader-Willi syndrome using PW71 methylation analysis--uniparental disomy and the significance of residual trisomy 15.
    Slater HR, Vaux C, Pertile M, Burgess T, Petrovic V.
    Prenat Diagn; 1997 Feb; 17(2):109-13. PubMed ID: 9061757
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  • 29. Poly-FISH: a technique of repeated hybridizations that improves cytogenetic analysis of fetal cells in maternal blood.
    Zhen DK, Wang JY, Falco VM, Weber W, Delli-Bovi L, Bianchi DW.
    Prenat Diagn; 1998 Nov; 18(11):1181-5. PubMed ID: 9854729
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  • 30. Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
    Micale MA, Wolff DJ, Dickerman LH, Redline R, Conroy JM, Schwartz S.
    Prenat Diagn; 1996 Oct; 16(10):893-7. PubMed ID: 8938057
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  • 31. Routine prenatal diagnosis of aneuploidy by FISH studies in high-risk pregnancies.
    Feldman B, Ebrahim SA, Hazan SL, Gyi K, Johnson MP, Johnson A, Evans MI.
    Am J Med Genet; 2000 Jan 31; 90(3):233-8. PubMed ID: 10678661
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  • 32. Screening for fetal chromosome aberrations in early pregnancy.
    Ferguson-Smith MA, Ferguson-Smith ME.
    J Clin Pathol Suppl (R Coll Pathol); 1976 Jan 31; 10():165-76. PubMed ID: 135003
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  • 33. Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment.
    Caine A, Maltby AE, Parkin CA, Waters JJ, Crolla JA, UK Association of Clinical Cytogeneticists (ACC).
    Lancet; 1976 Jan 31; 366(9480):123-8. PubMed ID: 16005334
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  • 34. [Prenatal diagnosis of chromosome aberrations after implementation of screening for Down's syndrome].
    Kjaergaard S, Hahnemann JM, Skibsted L, Jensen LN, Sperling L, Zingenberg H, Kristiansen A, Brøndum-Nielsen K.
    Ugeskr Laeger; 2008 Mar 31; 170(14):1152-6. PubMed ID: 18405480
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  • 35. Optimized criteria for using fluorescence in situ hybridization in the prenatal diagnosis of common aneuploidies.
    Leclercq S, Lebbar A, Grange G, Tsatsaris V, Le Tessier D, Dupont JM.
    Prenat Diagn; 2008 Apr 31; 28(4):313-8. PubMed ID: 18306148
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  • 36. Minimally-invasive early prenatal diagnosis using fluorescence in situ hybridization on samples from uterine lavage.
    Chang SD, Lin SL, Chu KK, Hsi BL.
    Prenat Diagn; 1997 Nov 31; 17(11):1019-25. PubMed ID: 9399349
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  • 37. Prenatal diagnosis by rapid aneuploidy detection and karyotyping: a prospective study of the role of ultrasound in 1589 second-trimester amniocenteses.
    Leung WC, Waters JJ, Chitty L.
    Prenat Diagn; 2004 Oct 31; 24(10):790-5. PubMed ID: 15503279
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  • 38. Interphase fluorescence in situ hybridization in a Turner syndrome variant with IsoXq. A case report.
    Chang SD, Lin SL, Chen FP, Chu KK.
    J Reprod Med; 1996 Mar 31; 41(3):175-8. PubMed ID: 8778416
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  • 39. Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier.
    Cotter PD, Musci TJ.
    Prenat Diagn; 2001 Mar 31; 21(3):171-5. PubMed ID: 11260602
    [Abstract] [Full Text] [Related]

  • 40. [Application of fluorescence in situ hybridization to prenatal diagnosis of Down syndrome].
    Wang M, Li QF, Qiao FY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun 31; 22(3):317-9. PubMed ID: 15952125
    [Abstract] [Full Text] [Related]

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