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310 related items for PubMed ID: 12210569

  • 1. Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.
    Graf MD, Gill P, Krew M, Schwartz S.
    Prenat Diagn; 2002 Aug; 22(8):645-8. PubMed ID: 12210569
    [Abstract] [Full Text] [Related]

  • 2. [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
    [Abstract] [Full Text] [Related]

  • 3. Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases.
    Weremowicz S, Sandstrom DJ, Morton CC, Niedzwiecki CA, Sandstrom MM, Bieber FR.
    Prenat Diagn; 2001 Apr; 21(4):262-9. PubMed ID: 11288114
    [Abstract] [Full Text] [Related]

  • 4. Residual risk for cytogenetic abnormalities after prenatal diagnosis by interphase fluorescence in situ hybridization (FISH).
    Homer J, Bhatt S, Huang B, Thangavelu M.
    Prenat Diagn; 2003 Jul; 23(7):566-71. PubMed ID: 12868085
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  • 6. Role of amniotic fluid interphase fluorescence in situ hybridization (FISH) analysis in patient management.
    Cheong Leung W, Chitayat D, Seaward G, Windrim R, Ryan G, Barrett J, Winsor EJ.
    Prenat Diagn; 2001 Apr; 21(4):327-32. PubMed ID: 11288128
    [Abstract] [Full Text] [Related]

  • 7. Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation.
    van den Berg C, Pijpers L, Halley DJ, Opstal DV, Los FJ.
    Am J Med Genet; 1999 Sep 10; 86(2):151-5. PubMed ID: 10449651
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  • 8. The clinical application of interphase FISH in prenatal diagnosis.
    Pergament E, Chen PX, Thangavelu M, Fiddler M.
    Prenat Diagn; 2000 Mar 10; 20(3):215-20. PubMed ID: 10719324
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  • 9. 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 10; 79(1):8-14. PubMed ID: 10646809
    [Abstract] [Full Text] [Related]

  • 10. [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 10; 25(5):538-41. PubMed ID: 18841567
    [Abstract] [Full Text] [Related]

  • 11. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].
    Steinborn A, Röddiger S, Born HJ, Baier P, Halberstadt E.
    Z Geburtshilfe Neonatol; 1996 Oct 10; 200(5):186-90. PubMed ID: 9035828
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  • 12. 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 10; 22(1):29-33. PubMed ID: 11810646
    [Abstract] [Full Text] [Related]

  • 13. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A, Kitsiou S, Fryssira H, Sofocleous C, Kouvidi E, Tsangaris GT, Salavoura K, Mavrou A.
    In Vivo; 2006 Jan 10; 20(4):473-8. PubMed ID: 16900777
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  • 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 10; 41(3):175-8. PubMed ID: 8778416
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  • 16. Maternal serum screening for fetal trisomy 18: benefits of patient-specific risk protocol.
    Hogge WA, Fraer L, Melegari T.
    Am J Obstet Gynecol; 2001 Aug 10; 185(2):289-93. PubMed ID: 11518881
    [Abstract] [Full Text] [Related]

  • 17. Efficacy of maternal serum screening in the prenatal detection of fetal chromosome abnormalities in Japanese women.
    Kishida T, Hoshi N, Hattori R, Negishi H, Yamada H, Okuyama K, Hanatani K, Takagi T, Sagawa T, Fujimoto S.
    Fetal Diagn Ther; 2000 Aug 10; 15(2):112-7. PubMed ID: 10720877
    [Abstract] [Full Text] [Related]

  • 18. 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 10; 124(8):1164-8. PubMed ID: 21542989
    [Abstract] [Full Text] [Related]

  • 19. Prenatal detection of isochromosome 21 by QF-PCR. A comparison between FISH and traditional karyotyping.
    Gole L, Lian NB, Lian NP, Rauff M, Biswas A, Choolani M.
    Fetal Diagn Ther; 2008 Apr 10; 24(1):47-50. PubMed ID: 18504381
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  • 20. Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis.
    Chen CP, Su JW, Chern SR, Kuo YL, Wu PS, Lee MS, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2015 Feb 10; 54(1):58-61. PubMed ID: 25675921
    [Abstract] [Full Text] [Related]

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