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Journal Abstract Search

307 related items for PubMed ID: 17654752

  • 1. False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite DNA probe (D18Z1) to the heterochromatic region of chromosome 9.
    Wei S, Siu VM, Decker A, Quigg MH, Roberson J, Xu J, Adeyinka A.
    Prenat Diagn; 2007 Nov; 27(11):1064-6. PubMed ID: 17654752
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  • 3. [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
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  • 5. Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha-satellite DNA probes: detection of a centromeric DNA break?
    Cantú ES, Khan TA, Pai GS.
    Am J Med Genet; 1992 Oct 01; 44(3):340-4. PubMed ID: 1488982
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  • 7. Potential use of buccal smears for rapid diagnosis of autosomal trisomy or chromosomal sex in newborn infants using DNA probes.
    Harris C, Wilkerson C, Clark K, Lazarski K, Meisner L.
    Am J Med Genet; 1994 Dec 01; 53(4):355-8. PubMed ID: 7864046
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  • 8. Prenatal diagnosis of partial trisomy through in situ hybridization on amniocytes with whole chromosome and centromere-specific DNA probes. A case report.
    Blancato JK, Eglinton G, George J, Benkendorf J, Pinckert T, Meck J.
    J Reprod Med; 1995 Jul 01; 40(7):537-9. PubMed ID: 7473445
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  • 9. [Non-radioactive in situ hybridization of alpha-satellite sequences in cytogenetic diagnosis].
    Perfumo C, Arslanian A, Zara F, Piombo G, Pierluigi M.
    Pathologica; 1992 Jul 01; 84(1091):363-9. PubMed ID: 1465321
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  • 10. [Possibilities for false-negative findings in trisomy 21 screening with FISH].
    Fritz B, Van Oorschot B, Latta E, Rehder H.
    Z Geburtshilfe Neonatol; 1996 Jul 01; 200(5):191-8. PubMed ID: 9035829
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  • 14. 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 01; 21(4):262-9. PubMed ID: 11288114
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  • 15. Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.
    Sullivan BA, Leana-Cox J, Schwartz S.
    Am J Med Genet; 1993 Aug 15; 47(2):223-30. PubMed ID: 8213910
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  • 18. [Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization].
    Solov'ev IV, Iurov IuB, Vorsanova SG, Marcais B, Rogaev EI, Kapanadze BI, Brodianskiĭ VM, Iankovskiĭ NK, Roizes G.
    Genetika; 1998 Nov 15; 34(11):1470-9. PubMed ID: 10096024
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