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Journal Abstract Search

147 related items for PubMed ID: 9602490

  • 1. High resolution chromosome analysis and in situ hybridization on amniotic fluid for diagnosis of a cryptic translocation.
    Guichet A, Briault S, Moraine C.
    Prenat Diagn; 1998 Apr; 18(4):399-403. PubMed ID: 9602490
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  • 2. Relevance to prenatal diagnosis of the identification of a human Y/autosome translocation by Y-chromosome-specific in situ hybridisation.
    Ellis PM, West JD, West KM, Murray RS, Coyle MC.
    Mol Reprod Dev; 1990 Jan; 25(1):37-41. PubMed ID: 2393582
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  • 3. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP, Devriendt K, Chern SR, Lee CC, Wang W, Lin SP.
    Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
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  • 6. Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier.
    Cotter PD, Musci TJ.
    Prenat Diagn; 2001 Mar; 21(3):171-5. PubMed ID: 11260602
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  • 7. [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ].
    Balícek P, Jüttnerová V, Jarosová M, Fialová J, Fiedler Z, Kolmanová J.
    Cas Lek Cesk; 2001 Mar 01; 140(4):122-4. PubMed ID: 11284430
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  • 8. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
    Senger G, Chudoba I, Friedrich U, Tommerup N, Claussen U, Brøndum-Nielsen K.
    Prenat Diagn; 1997 Apr 01; 17(4):369-74. PubMed ID: 9160390
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  • 9. [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 01; 25(5):538-41. PubMed ID: 18841567
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  • 10. Exclusion of uniparental inheritance of chromosome 15 in a fetus with a familial dicentric (Y;15) translocation.
    White LM, Treat K, Leff A, Styers D, Mitchell M, Knoll JH.
    Prenat Diagn; 1998 Feb 01; 18(2):111-6. PubMed ID: 9516010
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  • 11. Prenatal detection of a de novo Yqh-acrocentric translocation.
    Ng LK, Kwok YK, Tang LY, Ng PP, Ghosh A, Lau ET, Tang MH.
    Clin Biochem; 2006 Mar 01; 39(3):219-23. PubMed ID: 16515778
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  • 12. Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features.
    Kleefstra T, van de Zande G, Merkx G, Mieloo H, Hoovers JM, Smeets D.
    Eur J Hum Genet; 2000 Aug 01; 8(8):637-40. PubMed ID: 10951526
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  • 14. [Prenatal diagnosis of two pregnancies with risk of chromosomal disorders].
    Cui YX, Huang B, Shi YC, Lu HY, Xia XY, Pan LJ, Huang YF.
    Zhonghua Nan Ke Xue; 2007 Jul 01; 13(7):624-7. PubMed ID: 17725307
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  • 17. A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.
    Mechoso B, Vaglio A, Quadrelli A, Mark HF, Huang XL, Milunsky A, Quadrelli R.
    Fetal Diagn Ther; 2007 Jul 01; 22(4):249-53. PubMed ID: 17369689
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  • 18. [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 01; 21(6):608-10. PubMed ID: 15583993
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