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Journal Abstract Search

248 related items for PubMed ID: 9526620

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  • 3. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J, Chernos J, Roland B.
    Am J Med Genet; 1997 Dec 19; 73(3):327-9. PubMed ID: 9415693
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  • 4. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z, Mihci E, Keser I, Karaali K, Berker S, Luleci G.
    Genet Couns; 2012 Dec 19; 23(2):239-47. PubMed ID: 22876583
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  • 6. [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].
    Xiao B, Zhang JM, Ji X, Jiang WT, Hu J, Tao J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun 19; 28(3):247-50. PubMed ID: 21644216
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  • 7. 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. Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13).
    Coco R, del Rey G.
    J Genet Hum; 1978 Dec 15; 26(4):303-10. PubMed ID: 752064
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  • 12. Partial duplication 8q12----q21.2 in two sibs with maternally derived insertional and reciprocal translocations: case reports and review of partial duplications of chromosome 8.
    Walker AP, Bocian M.
    Am J Med Genet; 1987 May 15; 27(1):3-22. PubMed ID: 3300332
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  • 16. Familial complex chromosome rearrangement giving rise to balanced and unbalanced recombination products.
    Zahed L, Der Kaloustian V, Batanian JR.
    Am J Med Genet; 1998 Aug 27; 79(1):30-4. PubMed ID: 9738865
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  • 18. Second meiotic nondisjunction of the rearranged chromosome in a familial reciprocal 5/13 translocation.
    Masuno M, Cholsong Y, Kuwahara T, Shimizu N, Yamaguchi S, Kawabata I, Tamaya T, Morishita Y, Yoshimi N, Orii T.
    Am J Med Genet; 1991 Oct 01; 41(1):32-4. PubMed ID: 1951460
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