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PUBMED FOR HANDHELDS

Journal Abstract Search


183 related items for PubMed ID: 2144840

  • 1. Segregation of acrocentric chromosome association in familial dicentric Robertsonian translocation t(14p;22p), aneuploidy (trisomy-21) and heteromorphism.
    Murthy DS, Sundareshan TS, Farag TI, al-Awadi SA, al-Othman SA.
    Indian J Exp Biol; 1990 Jun; 28(6):511-5. PubMed ID: 2144840
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  • 3. [Molecular cytogenetic study of Robertsonian translocation 13;14 and Down syndrome in a 3-year-old infant].
    Iurov IIu, Vorsanova SG, Monakhov VV, Beresheva AK, Solov'ev IV, Iurov IuB.
    Tsitol Genet; 2004 Jun; 38(6):54-9. PubMed ID: 15882036
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  • 4. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.
    Pazarbaşi A, Demirhan O, Turgut M, Güzel I, Taştemir D.
    Genet Couns; 2008 Jun; 19(3):301-8. PubMed ID: 18990986
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  • 6. Familial robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21.
    Mau UA, Petruch UR, Kaiser P, Eggermann T.
    Eur J Hum Genet; 2000 Nov; 8(11):815-9. PubMed ID: 11093270
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  • 7. Meiotic segregation of rare Robertsonian translocations: sperm analysis of three t(14q;22q) cases.
    Moradkhani K, Puechberty J, Bhatt S, Vago P, Janny L, Lefort G, Hamamah S, Sarda P, Pellestor F.
    Hum Reprod; 2006 May; 21(5):1166-71. PubMed ID: 16439506
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  • 9. [Chromosome analyses in parents of children with trisomy 21[].
    Mattei JF, Giraud F.
    J Genet Hum; 1975 Oct; 23 SUPPL():31-41. PubMed ID: 129538
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  • 12. A familial reciprocal translocation t(1;15) in three generations identified in a regular trisomy 21 patient.
    García-Delgado C, Bahena-Martínez E, Aparicio-Onofre A, Guevara-Yañez R, Cervantes-Peredo A, Azotla-Vilchis OC, Estrada-Mena J, Luna-Angulo A, Villa-Morales J, Moran-Barroso VF.
    Genet Couns; 2010 Oct; 21(3):299-306. PubMed ID: 20964121
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