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183 related items for PubMed ID: 17899566

  • 1. High-density array comparative genomic hybridization analysis and follow-up of a child with a de novo complex chromosome rearrangement detected prenatally.
    Quadrelli A, Vaglio A, Quadrelli R, Mechoso B, Fan YS, Huang T.
    Prenat Diagn; 2007 Oct; 27(10):982-3. PubMed ID: 17899566
    [No Abstract] [Full Text] [Related]

  • 2. 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 Oct; 22(4):249-53. PubMed ID: 17369689
    [Abstract] [Full Text] [Related]

  • 3. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q).
    Mercier S, Fellmann F, Cattin J, Bresson JL.
    Prenat Diagn; 1996 Nov; 16(11):1046-50. PubMed ID: 8953640
    [Abstract] [Full Text] [Related]

  • 4. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.
    Peschka B, Leygraaf J, Hansmann D, Hansmann M, Schröck E, Ried T, Engels H, Schwanitz G, Schubert R.
    Prenat Diagn; 1999 Dec; 19(12):1143-9. PubMed ID: 10590433
    [Abstract] [Full Text] [Related]

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  • 7. 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 Dec; 20(4):473-8. PubMed ID: 16900777
    [Abstract] [Full Text] [Related]

  • 8. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
    Suzumori K, Tanemura M, Oya N, Suzumori N, Kim KC, Ohashi H, Fukushima Y.
    Prenat Diagn; 1998 Jul; 18(7):725-30. PubMed ID: 9706655
    [Abstract] [Full Text] [Related]

  • 9. De novo complex chromosome rearrangement: a study of two patients.
    Melo DG, Huber J, Giuliani LR, Mazzucatto LF, Riegel M, Pina-Neto JM.
    Genet Couns; 2004 Jul; 15(3):303-10. PubMed ID: 15517822
    [Abstract] [Full Text] [Related]

  • 10. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH).
    Hoffman DJ, Punnett HH, Pyeritz RE.
    Am J Perinatol; 2004 Feb; 21(2):69-71. PubMed ID: 15017469
    [Abstract] [Full Text] [Related]

  • 11. Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up.
    Kim JJ, Rhee HS, Chung YT, Park SY, Choi SK.
    Exp Mol Med; 1999 Sep 30; 31(3):134-6. PubMed ID: 10551261
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis of an extra der(4) resulting from a complex maternal chromosome translocation.
    Migliori MV, Pettinari A, Ciaschini AM, Piermattei P, Pigliapoco F, Discepoli G.
    Prenat Diagn; 2004 Apr 30; 24(4):290-2. PubMed ID: 15065104
    [Abstract] [Full Text] [Related]

  • 13. De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome.
    Yakut S, Cetin Z, Berker-Karauzum S, Mihci E, Mendilcioglu I, Luleci G.
    Genet Couns; 2011 Apr 30; 22(1):63-8. PubMed ID: 21614990
    [Abstract] [Full Text] [Related]

  • 14. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder.
    Goumy C, Mihaescu M, Tchirkov A, Giollant M, Benier C, Francannet C, Jaffray JY, Geneix A, Vago P.
    Genet Couns; 2006 Apr 30; 17(3):371-9. PubMed ID: 17100206
    [Abstract] [Full Text] [Related]

  • 15. High-density genome array is superior to fluorescence in-situ hybridization analysis of monosomy 3 in choroidal melanoma fine needle aspiration biopsy.
    Young TA, Burgess BL, Rao NP, Gorin MB, Straatsma BR.
    Mol Vis; 2007 Dec 21; 13():2328-33. PubMed ID: 18199974
    [Abstract] [Full Text] [Related]

  • 16. Familial complex chromosomal rearrangement resulting in a recombinant chromosome.
    Berend SA, Bodamer OA, Shapira SK, Shaffer LG, Bacino CA.
    Am J Med Genet; 2002 May 15; 109(4):311-7. PubMed ID: 11992486
    [Abstract] [Full Text] [Related]

  • 17. Prenatal detection of extra structurally abnormal chromosomes (ESACs): new cases and a review of the literature.
    Hastings RJ, Nisbet DL, Waters K, Spencer T, Chitty LS.
    Prenat Diagn; 1999 May 15; 19(5):436-45. PubMed ID: 10360512
    [Abstract] [Full Text] [Related]

  • 18. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.
    Law LW, Lau TK, Fung TY, Leung TY, Wang CC, Choy KW.
    BJOG; 2009 Jan 15; 116(2):339-43. PubMed ID: 19018765
    [Abstract] [Full Text] [Related]

  • 19. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Chern SR, Lee CC, Chen YJ, Wang W.
    Prenat Diagn; 2005 Dec 15; 25(12):1170-2. PubMed ID: 16315335
    [No Abstract] [Full Text] [Related]

  • 20. A rare case of de novo distal 19q trisomy prenatally diagnosed.
    Rombout S, Sartenaer D, Parmentier B, Dugauquier C, Gillerot Y.
    Prenat Diagn; 2004 Oct 15; 24(10):822-7. PubMed ID: 15503276
    [Abstract] [Full Text] [Related]

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