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Journal Abstract Search

131 related items for PubMed ID: 8713667

  • 21.
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  • 22. [Possibilities for false-negative findings in trisomy 21 screening with FISH].
    Fritz B, Van Oorschot B, Latta E, Rehder H.
    Z Geburtshilfe Neonatol; 1996; 200(5):191-8. PubMed ID: 9035829
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  • 25. Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cells.
    Bryndorf T, Christensen B, Xiang Y, Lind AM, Philip J.
    Prenat Diagn; 1993 Sep; 13(9):815-23. PubMed ID: 8278312
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  • 30. Detection of chromosomal abnormalities using fluorescence in situ hybridization (FISH).
    Jobanputra V, Kriplani A, Choudhry VP, Kucheria K.
    Natl Med J India; 1998 Sep; 11(6):259-63. PubMed ID: 10083791
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  • 32. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP, Chern SR, Wang W, Lee CC, Chen WL, Chen LF, Chang TY, Tzen CY.
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
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  • 38. Detection of Down syndrome by in situ hybridization with chromosome 21 specific DNA probes.
    Lichter P, Jauch A, Cremer T, Ward DC.
    Prog Clin Biol Res; 1990 May; 360():69-78. PubMed ID: 2147290
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  • 39. Fluorescence in situ hybridization in prenatal screening: lessons from an inherited chromosome 18 marker.
    Valentin M, Ottenwalter A, Serero S, Muller F, Luton D, Ducarme G.
    Prenat Diagn; 2009 Dec; 29(12):1177-9. PubMed ID: 19816880
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  • 40.
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