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246 related items for PubMed ID: 8183853

  • 1. Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization.
    Cacheux V, Tachdjian G, Druart L, Oury JF, Sérero S, Blot P, Nessmann C.
    Prenat Diagn; 1994 Feb; 14(2):79-86. PubMed ID: 8183853
    [Abstract] [Full Text] [Related]

  • 2. Role of multicolor fluorescence in situ hybridization (FISH) in simultaneous detection of probe sets for chromosome 18, X and Y in uncultured amniotic fluid cells.
    Kim JI, Rhee JH.
    J Korean Med Sci; 1999 Aug; 14(4):438-42. PubMed ID: 10485625
    [Abstract] [Full Text] [Related]

  • 3. Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells.
    Ried T, Landes G, Dackowski W, Klinger K, Ward DC.
    Hum Mol Genet; 1992 Aug; 1(5):307-13. PubMed ID: 1303206
    [Abstract] [Full Text] [Related]

  • 4. Cross-hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common chromosomal aneuploidies by FISH.
    Verlinsky Y, Ginsberg N, Chmura M, Freidine M, White M, Strom C, Kuliev A.
    Prenat Diagn; 1995 Sep; 15(9):831-4. PubMed ID: 8559753
    [Abstract] [Full Text] [Related]

  • 5. Quantitative evaluation of fluorescence in situ hybridization (FISH) signals in uncultured coelomic cells.
    Crüger DG, Bruun-Petersen G, Kølvraa S.
    Prenat Diagn; 1997 Jul; 17(7):635-42. PubMed ID: 9249864
    [Abstract] [Full Text] [Related]

  • 6. Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).
    Witters I, Devriendt K, Legius E, Matthijs G, Van Schoubroeck D, Van Assche FA, Fryns JP.
    Prenat Diagn; 2002 Jan; 22(1):29-33. PubMed ID: 11810646
    [Abstract] [Full Text] [Related]

  • 7. [Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization].
    Wang H, Li H, Wang H, Wang H, Xia Y, Wen J, Long Z, Dai H, Liang D, Xia J, Wu L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):538-41. PubMed ID: 18841567
    [Abstract] [Full Text] [Related]

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  • 9. [Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization].
    Xiao HM, Tan YQ, Li LY, Lu GX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):608-10. PubMed ID: 15583993
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  • 11. [Application of inter-fluorescence in situ hybridization of chromosome 13/21 alpha satellite probe in amniotic cells for prenatal diagnosis trisomy 21 syndrome].
    Li W, Wu Y, Ye Z.
    Zhonghua Fu Chan Ke Za Zhi; 2001 Feb; 36(2):76-8. PubMed ID: 11783350
    [Abstract] [Full Text] [Related]

  • 12. Fluorescence in situ hybridization in uncultured amniocytes for detection of aneuploidy in 4210 prenatal cases.
    Jia CW, Wang SY, Ma YM, Lan YL, Si YM, Yu L, Zhou LY.
    Chin Med J (Engl); 2011 Apr; 124(8):1164-8. PubMed ID: 21542989
    [Abstract] [Full Text] [Related]

  • 13. Detection of newborn aneuploidy by interphase fluorescence in situ hybridization.
    Jalal SM, Law ME.
    Mayo Clin Proc; 1997 Aug; 72(8):705-10. PubMed ID: 9276596
    [Abstract] [Full Text] [Related]

  • 14. Simultaneous identification of chromosomes 18, X and Y in uncultured amniocytes by using multi-primed in situ labelling technique.
    Gadji M, Krabchi K, Drouin R.
    Clin Genet; 2005 Jul; 68(1):15-22. PubMed ID: 15952981
    [Abstract] [Full Text] [Related]

  • 15. 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; 41(3):175-8. PubMed ID: 8778416
    [Abstract] [Full Text] [Related]

  • 16. Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples.
    Bryndorf T, Lundsteen C, Lamb A, Christensen B, Philip J.
    Acta Obstet Gynecol Scand; 2000 Jan; 79(1):8-14. PubMed ID: 10646809
    [Abstract] [Full Text] [Related]

  • 17. Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens.
    Ward BE, Gersen SL, Carelli MP, McGuire NM, Dackowski WR, Weinstein M, Sandlin C, Warren R, Klinger KW.
    Am J Hum Genet; 1993 May; 52(5):854-65. PubMed ID: 8488836
    [Abstract] [Full Text] [Related]

  • 18. A prospective comparative study on fluorescence in situ hybridization (FISH) of uncultured amniocytes and standard karyotype analysis.
    Eiben B, Trawicki W, Hammans W, Goebel R, Epplen JT.
    Prenat Diagn; 1998 Sep; 18(9):901-6. PubMed ID: 9793971
    [Abstract] [Full Text] [Related]

  • 19. Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial.
    Bryndorf T, Christensen B, Vad M, Parner J, Brocks V, Philip J.
    Prenat Diagn; 1997 Apr; 17(4):333-41. PubMed ID: 9160386
    [Abstract] [Full Text] [Related]

  • 20. Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes.
    Kuo WL, Tenjin H, Segraves R, Pinkel D, Golbus MS, Gray J.
    Am J Hum Genet; 1991 Jul; 49(1):112-9. PubMed ID: 2063863
    [Abstract] [Full Text] [Related]

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