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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

190 related items for PubMed ID: 9160390

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  • 3. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
    Cora T, Acar H, Oran B.
    Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
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  • 5. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ.
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
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  • 10. Rapid generation of region specific probes by chromosome microdissection and their application.
    Meltzer PS, Guan XY, Burgess A, Trent JM.
    Nat Genet; 1992 Apr; 1(1):24-8. PubMed ID: 1301994
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  • 13. Duplication of chromosome region 8p23.1-->p23.3: a benign variant?
    Engelen JJ, Moog U, Evers JL, Dassen H, Albrechts JC, Hamers AJ.
    Am J Med Genet; 2000 Mar 06; 91(1):18-21. PubMed ID: 10751083
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  • 16. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
    Koochek M, Harvard C, Hildebrand MJ, Van Allen M, Wingert H, Mickelson E, Holden JJ, Rajcan-Separovic E, Lewis ME.
    Clin Genet; 2006 Feb 06; 69(2):124-34. PubMed ID: 16433693
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  • 17. Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).
    Santolaya-Forgas J, De Leon J, Powell WC, Tonk V.
    Prenat Diagn; 2004 Mar 06; 24(3):209-12. PubMed ID: 15057955
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  • 20. Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization.
    Engelen JJ, Loots WJ, Albrechts JC, Plomp AS, van der Meer SB, Vles JS, Hamers GJ, Geraedts JP.
    Am J Med Genet; 1998 Feb 03; 75(4):409-13. PubMed ID: 9482648
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