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Journal Abstract Search

357 related items for PubMed ID: 15017469

  • 1. 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
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  • 5. A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.
    Gibson LH, McGrath J, Yang-Feng TL.
    Am J Med Genet; 1997 Feb 11; 68(4):417-20. PubMed ID: 9021014
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  • 7. Prenatal detection of deletion 6q13q15 in a complex karyotype.
    Yu M, Obringer AC, Fowler MH, Hummel M, Wenger SL.
    Prenat Diagn; 2005 Dec 11; 25(12):1084-7. PubMed ID: 16231325
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  • 8. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO, Karauzum SB, Mihci E, Tacoy S, Luleci G.
    Genet Couns; 2005 Dec 11; 16(2):129-38. PubMed ID: 16080292
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  • 9. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.
    Celep F, Acar H, Aynaci O, Aynaci FM, Karagüzel A.
    Genet Couns; 2001 Dec 11; 12(4):319-26. PubMed ID: 11837600
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  • 11. Complex familial rearrangement of chromosome 9p24.3 detected by FISH.
    Repetto GM, Wagstaff J, Korf BR, Knoll JH.
    Am J Med Genet; 1998 Apr 01; 76(4):306-9. PubMed ID: 9545094
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  • 18. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z, Mihci E, Keser I, Karaali K, Berker S, Luleci G.
    Genet Couns; 2012 Apr 01; 23(2):239-47. PubMed ID: 22876583
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  • 19. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
    Karmous-Benailly H, Giuliano F, Massol C, Bloch C, De Ricaud D, Lambert JC, Perelman S.
    Eur J Med Genet; 2006 Apr 01; 49(5):431-8. PubMed ID: 16497571
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  • 20. 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 01; 26(6):565-70. PubMed ID: 16683274
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