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Journal Abstract Search

387 related items for PubMed ID: 10740198

  • 1. An assessment of the use of interphase FISH with chromosome specific probes as an alternative to cytogenetics in prenatal diagnosis.
    Thein AT, Abdel-Fattah SA, Kyle PM, Soothill PW.
    Prenat Diagn; 2000 Apr; 20(4):275-80. PubMed ID: 10740198
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  • 2. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP, Wu JP, Li XT, Lei CX, Xu JZ, Yin M.
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
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  • 4. The clinical application of interphase FISH in prenatal diagnosis.
    Pergament E, Chen PX, Thangavelu M, Fiddler M.
    Prenat Diagn; 2000 Mar; 20(3):215-20. PubMed ID: 10719324
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  • 5. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
    Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Lai ST, Yang CW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):545-549. PubMed ID: 28805616
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  • 6. First-trimester prenatal diagnosis performed on pregnant women with fetal ultrasound abnormalities: the reliability of interphase fluorescence in situ hybridization (FISH) on mesenchymal core for the main aneuploidies.
    Toutain J, Epiney M, Begorre M, Dessuant H, Vandenbossche F, Horovitz J, Saura R.
    Eur J Obstet Gynecol Reprod Biol; 2010 Apr; 149(2):143-6. PubMed ID: 20045588
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  • 7. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
    Ulmer R, Pfeiffer RA, Kollert A, Beinder E.
    Z Geburtshilfe Neonatol; 2000 Apr; 204(1):1-7. PubMed ID: 10721179
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  • 10. [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 Apr; 200(5):186-90. PubMed ID: 9035828
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  • 11. Prenatal diagnosis of mosaicism for double aneuploidy of 47,XXY and trisomy 7 (48,XXY,+7) at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP, Tsai HT, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Town DD, Chen WL, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2021 May; 60(3):543-548. PubMed ID: 33966745
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  • 12. Prenatal screening for fetal aneuploidy in singleton pregnancies.
    Chitayat D, Langlois S, Douglas Wilson R, SOGC GENETICS COMMITTEE, CCMG PRENATAL DIAGNOSIS COMMITTEE.
    J Obstet Gynaecol Can; 2011 Jul; 33(7):736-750. PubMed ID: 21749752
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  • 16. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.
    Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2013 Sep; 52(3):395-400. PubMed ID: 24075380
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  • 18. Rapid one-day fluorescence in situ hybridisation in prenatal diagnosis using uncultured amniocytes and chorionic villi.
    Cai LS, Lim AS, Tan A.
    Ann Acad Med Singap; 1999 Jul; 28(4):502-7. PubMed ID: 10561761
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  • 19. Prenatal cytogenetic diagnosis study of 2782 cases of high-risk pregnant women.
    Zhang L, Zhang XH, Liang MY, Ren MH.
    Chin Med J (Engl); 2010 Feb 20; 123(4):423-30. PubMed ID: 20193481
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  • 20. [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 20; 47(11):808-12. PubMed ID: 23302119
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