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PUBMED FOR HANDHELDS

Journal Abstract Search

157 related items for PubMed ID: 16193462

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  • 2. 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
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  • 4. Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion.
    Prontera P, Aiello V, Toschi M, Turci A, Gruppioni R, Buldrini B, Zago S, Bonfatti A, Donti E, Calzolari E, Sensi A.
    Genet Couns; 2007 Feb; 18(3):309-15. PubMed ID: 18019372
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  • 9. Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin.
    López-Exposito I, Guillén-Navarro E, Bafallíu JA, Bernabé MC, Escalona A, Fuster C.
    Eur J Med Genet; 2006 Feb; 49(6):511-5. PubMed ID: 16824814
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  • 10. Balanced de novo translocation t(6;7)(p25;q31) and cleft palate as an isolated finding.
    Balci S, Aypar E, Son YA, Beksaç MS.
    Genet Couns; 2004 Feb; 15(3):317-20. PubMed ID: 15517824
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  • 11. Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities.
    Reynolds PA, Powlesland RM, Keen TJ, Inglehearn CF, Cunningham AF, Green ED, Brown KW.
    Genes Chromosomes Cancer; 1996 Nov; 17(3):151-5. PubMed ID: 8946193
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  • 12. Prenatal diagnosis of del(9)(p24): a sex reverse case.
    Privitera O, Vessecchia G, Bernasconi B, Bettio D, Stioui S, Giordano G.
    Prenat Diagn; 2005 Oct; 25(10):945-8. PubMed ID: 16086437
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  • 13. Prenatal diagnosis of interstitially satellited 6p.
    Chen CP, Chern SR, Lee CC, Chen WL, Wang W.
    Prenat Diagn; 2004 Jun; 24(6):430-3. PubMed ID: 15229841
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  • 18. Fetal ventriculomegaly, agenesis of the corpus callosum and chromosomal translocation--case report.
    Amato M, Howald H, von Muralt G.
    J Perinat Med; 1986 Jun; 14(4):271-4. PubMed ID: 3546665
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  • 19. Double autosomal trisomy (1q21.2----qter and 14pter----q13) in a female fetus with nuchal oedema.
    Fryns JP, Kleczkowska A, Moerman P, van den Berghe K, van den Berghe H.
    Ann Genet; 1987 Jun; 30(4):240-2. PubMed ID: 3501268
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  • 20. Prenatal diagnosis of occipital encephalocele, mega-cisterna magna, mesomelic shortening, and clubfeet associated with pure tetrasomy 20p.
    Wu YC, Fang JS, Lee KF, Estipona J, Yang ML, Yuan CC.
    Prenat Diagn; 2003 Feb; 23(2):124-7. PubMed ID: 12575018
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