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540 related items for PubMed ID: 17369689

  • 1. 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; 22(4):249-53. PubMed ID: 17369689
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
    Giardino D, Corti C, Ballarati L, Finelli P, Valtorta C, Botta G, Giudici M, Grosso E, Larizza L.
    Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 Dec; 17(3):371-9. PubMed ID: 17100206
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
    Simovich MJ, Yatsenko SA, Kang SH, Cheung SW, Dudek ME, Pursley A, Ward PA, Patel A, Lupski JR.
    Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
    [Abstract] [Full Text] [Related]

  • 9. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: two new cases and review of the literature.
    Ruiz C, Grubs RE, Jewett T, Cox-Jones K, Abruzzese E, Pettenati MJ, Rao PN.
    Am J Med Genet; 1996 Aug 23; 64(3):478-84. PubMed ID: 8862625
    [Abstract] [Full Text] [Related]

  • 10. 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 Aug 23; 15(3):303-10. PubMed ID: 15517822
    [Abstract] [Full Text] [Related]

  • 11. 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 Aug 23; 20(4):473-8. PubMed ID: 16900777
    [Abstract] [Full Text] [Related]

  • 12. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
    Tan YQ, Di YF, Song YZ, Cheng DH, Li LY, Lu GX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 23; 24(4):392-6. PubMed ID: 17680527
    [Abstract] [Full Text] [Related]

  • 13. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
    Ballarati L, Recalcati MP, Bedeschi MF, Lalatta F, Valtorta C, Bellini M, Finelli P, Larizza L, Giardino D.
    Eur J Med Genet; 2009 Aug 23; 52(4):218-23. PubMed ID: 19236961
    [Abstract] [Full Text] [Related]

  • 14. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16.
    Phelan MC, Blackburn W, Rogers RC, Crawford EC, Cooley NR, Schrock E, Ning Y, Ried T.
    Prenat Diagn; 1998 Nov 23; 18(11):1174-80. PubMed ID: 9854728
    [Abstract] [Full Text] [Related]

  • 15. 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 23; 21(2):69-71. PubMed ID: 15017469
    [Abstract] [Full Text] [Related]

  • 16. 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 23; 18(7):725-30. PubMed ID: 9706655
    [Abstract] [Full Text] [Related]

  • 17. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
    Zunino A, Viaggi S, Ottaggio L, Fronza G, Schenone A, Roncella S, Abbondandolo A.
    Haematologica; 2000 Mar 23; 85(3):250-5. PubMed ID: 10702812
    [Abstract] [Full Text] [Related]

  • 18. M-FISH applications in clinical genetics.
    Cetin Z, Berker Karaüzüm S, Yakut S, Mihçi E, Baumer A, Wey E, Taçoy S, Bağci G, Lüleci G.
    Genet Couns; 2005 Mar 23; 16(3):257-68. PubMed ID: 16259323
    [Abstract] [Full Text] [Related]

  • 19. Cytogenetic study of a patient with infant acute lymphoblastic leukemia using GTG-banding and chromosome painting.
    Alter D, Mark HF.
    Exp Mol Pathol; 2000 Oct 23; 69(2):152-8. PubMed ID: 11001863
    [Abstract] [Full Text] [Related]

  • 20. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP, Chen M, Su YN, Huang JP, Ma GC, Chang SP, Chern SR, Chen YT, Su JW, Lee CC, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2012 Jun 23; 51(2):245-52. PubMed ID: 22795102
    [Abstract] [Full Text] [Related]

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