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Journal Abstract Search

151 related items for PubMed ID: 3379383

  • 1.
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  • 2. [Diagnosis of minor chromosome modifications by molecular cytogenetics].
    Taviaux S, Moncla A, Giraud F, Demaille J, Mattei JF, Mattei MG.
    Ann Genet; 1989; 32(4):204-10. PubMed ID: 2610486
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  • 3. 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; 19(3):301-8. PubMed ID: 18990986
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  • 4. Reproductive risk in mating between two translocation carriers: case report and review of the literature.
    Tsuji K, Narahara K, Yokoyama Y, Ninomiya S, Yonesawa S, Hiramatsu Y, Masaoka H, Kudo N, Seino Y.
    Am J Med Genet; 1993 Jun 15; 46(5):524-8. PubMed ID: 8322814
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  • 8. Direct and inverted reciprocal chromosome insertions between chromosomes 7 and 14 in a woman with recurrent miscarriages.
    Wang YT, Bajalica S, Han FY, Wang ZC, Bui TH, Xie YG.
    Am J Med Genet; 1994 Sep 01; 52(3):349-51. PubMed ID: 7810568
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  • 9. Translocation t(22;22)(p11.1;q11.1) and NOR studies in a female with a history of repeated fetal loss.
    Multani AS, Radhakrishna U, Sheth FJ, Shah VC, Chinoy NJ.
    Ann Genet; 1992 Sep 01; 35(2):105-9. PubMed ID: 1524406
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  • 10. De novo complex chromosomal rearrangement in a woman with recurrent spontaneous abortion and one healthy daughter.
    Timár L, Béres J, Kosztolányi G, Németh I.
    Hum Genet; 1991 Feb 01; 86(4):421. PubMed ID: 1999348
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  • 11. Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18.
    Lee MH, Park SY, Kim YM, Kim JM, Han JY, Kim MY, Ryu HM.
    Prenat Diagn; 2002 Feb 01; 22(2):102-4. PubMed ID: 11857612
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  • 12. Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection.
    Benn PA, Hsu LY, Verma RS, Alonso ML, Reich E, Wishnick M.
    Obstet Gynecol; 1987 Sep 01; 70(3 Pt 2):449-52. PubMed ID: 3627600
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  • 13. Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11).
    Fryns JP, Kleczkowska A.
    Ann Genet; 1987 Sep 01; 30(2):109-10. PubMed ID: 3499841
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  • 16. [A de novo complex chromosomal rearrangement including translocation on 1,5 and 12 in a female carrier with her healthy girl].
    Cui YX, Wang YM, Yao B, Huang YF.
    Yi Chuan; 2004 Sep 01; 26(5):612-4. PubMed ID: 15640072
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  • 17. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18.
    Chen CP, Lin CC, Su YN, Tsai FJ, Chen JT, Chern SR, Lee CC, Town DD, Chen LF, Wu PC, Wang W.
    Taiwan J Obstet Gynecol; 2010 Jun 01; 49(2):188-91. PubMed ID: 20708526
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  • 18. Chromosome 19; 20 reciprocal translocation.
    Jayakaran F, Tilak P, Rajangam SM, Thomas IM.
    J Postgrad Med; 2002 Jun 01; 48(1):71. PubMed ID: 12082336
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  • 19. Chromosome analysis in cases with repeated spontaneous abortions.
    Neu RL, Entes K, Bannerman RM.
    Obstet Gynecol; 1979 Mar 01; 53(3):373-5. PubMed ID: 424112
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  • 20. Trisomy 20p from maternal translocation and anencephaly. Case report and genetic review.
    Zumel RM, Darnaude MT, Delicado A, Diaz de Bustamante A, de Torres ML, López Pajares I.
    Ann Genet; 1989 Mar 01; 32(4):247-9. PubMed ID: 2610493
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