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Journal Abstract Search

583 related items for PubMed ID: 17100206

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  • 2. 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; 49(5):431-8. PubMed ID: 16497571
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  • 3. 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; 52(4):218-23. PubMed ID: 19236961
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  • 4. 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
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  • 5. The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.
    Gribble SM, Prigmore E, Burford DC, Porter KM, Ng BL, Douglas EJ, Fiegler H, Carr P, Kalaitzopoulos D, Clegg S, Sandstrom R, Temple IK, Youings SA, Thomas NS, Dennis NR, Jacobs PA, Crolla JA, Carter NP.
    J Med Genet; 2005 Jan 15; 42(1):8-16. PubMed ID: 15635069
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  • 6. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification.
    Guilherme RS, Cernach MC, Sfakianakis TE, Takeno SS, Nardozza LM, Rossi C, Bhatt SS, Liehr T, Melaragno MI.
    Cytogenet Genome Res; 2013 Jan 15; 141(4):317-23. PubMed ID: 23817307
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  • 10. 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 15; 26(6):565-70. PubMed ID: 16683274
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  • 13. 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 15; 19(12):1143-9. PubMed ID: 10590433
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  • 14. Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.
    Röthlisberger B, Kotzot D, Brecevic L, Koehler M, Balmer D, Binkert F, Schinzel A.
    Eur J Hum Genet; 1999 Dec 15; 7(8):873-83. PubMed ID: 10602362
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  • 18. 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 15; 26(2):138-46. PubMed ID: 16470734
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  • 19. 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 Feb 15; 15(3):303-10. PubMed ID: 15517822
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  • 20. 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
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