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Journal Abstract Search

234 related items for PubMed ID: 23431746

  • 1. A de novo translocation of chromosomes 1 and 2 in an 18 year old boy with syndromic mental retardation.
    Neetha J, Girisha KM, Gopinath PM, Sekhar MR.
    Genet Couns; 2012; 23(4):473-6. PubMed ID: 23431746
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  • 2. 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; 15(3):303-10. PubMed ID: 15517822
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  • 7. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
    Tatar A, Oztas S, Yakut T, Ors R.
    Genet Couns; 2005; 16(2):173-7. PubMed ID: 16080298
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  • 10. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
    Akbas E, Polat S, Karakas-Celik S, Altintas ZM, Yildirim M, Yilgor E.
    Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
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  • 11. De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia.
    Magri C, Piovani G, Pilotta A, Michele T, Buzi F, Barlati S.
    Eur J Med Genet; 2011; 54(3):361-4. PubMed ID: 21211576
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  • 18. [Unusual chromosome translocation 46, XX, t(1;16) (p13;p13) as a possible cause of retarded development of carrier].
    Nefić H.
    Med Arh; 2004; 58(4):199-201. PubMed ID: 15526583
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  • 19. A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability.
    Cobben JM, Weiss MM, van Dijk FS, De Reuver R, de Kruiff C, Pondaag W, Hennekam RC, Yntema HG.
    Eur J Med Genet; 2014; 57(11-12):636-8. PubMed ID: 25281490
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  • 20. 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; 16(2):129-38. PubMed ID: 16080292
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