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Journal Abstract Search

307 related items for PubMed ID: 9147887

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  • 5. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.
    Prabhakara K, Wyandt HE, Huang XL, Prasad KS, Ramadevi AR.
    Ann Genet; 2004; 47(3):297-303. PubMed ID: 15337476
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  • 6. Recombinant chromosome 18 resulting from a maternal pericentric inversion.
    Ayukawa H, Tsukahara M, Fukuda M, Kondoh O.
    Am J Med Genet; 1994 May 01; 50(4):323-5. PubMed ID: 8209910
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  • 7. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC, Carnevale A, Gómez L, del Castillo V, Frías S.
    Rev Invest Clin; 1996 May 01; 48(1):27-33. PubMed ID: 8815483
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  • 12. 9p deletion and distal 9q duplication due to a paternal pericentric inversion 9(p22q32).
    Sonoda T, Ohba K, Ohdo S, Sameshima K.
    Jinrui Idengaku Zasshi; 1991 Mar 01; 36(1):111-6. PubMed ID: 2062007
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  • 13. The 18p- syndrome. Report of five cases.
    Zumel RM, Darnaude MT, Delicado A, Diaz de Bustamante A, de Torres ML, López-Pájares I.
    Ann Genet; 1989 Mar 01; 32(3):160-3. PubMed ID: 2817777
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  • 17. Familial pericentric inversion of chromosome 8.
    Sujansky E, Smith AC, Peakman DC, McConnell TS, Baca P, Robinson A.
    Am J Med Genet; 1981 Mar 01; 10(3):229-35. PubMed ID: 6171164
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  • 19. Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion 5(p15.1q35.1).
    Sonoda T, Kawaguchi K, Ohba K, Madokoro H, Ohdo S.
    Jinrui Idengaku Zasshi; 1989 Jun 01; 34(2):129-34. PubMed ID: 2671452
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