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Journal Abstract Search

197 related items for PubMed ID: 2302035

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  • 2. 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; 23(2):239-47. PubMed ID: 22876583
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  • 4. Tetrasomy 9p caused by idic (9) (pter----q13----pter).
    Cavalcanti DP, Ferrari I, de Almeida JC, de Pina Neto JM, de Oliveira JA.
    Am J Med Genet; 1987 Jul; 27(3):497-503. PubMed ID: 3631125
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  • 9. Combined trisomy 9P and Shprintzen syndrome resulting from a paternal t(9;22).
    Komatsu H, Kihara A, Komura E, Mitsufuji N, Tsujii H, Kakita S, Ikuta H.
    Genet Couns; 2001 Jul; 12(2):137-43. PubMed ID: 11491308
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  • 12. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP, Kleczkowska A, Jaeken J, Van Herck K, Van den Berghe MH.
    Ann Genet; 1989 Jul; 32(3):177-9. PubMed ID: 2486064
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  • 14. Type and contretype signs in monosomy and trisomy 9p. On a case 46,XY, del (9) (pter yields p12:).
    Hernandez A, Rivera H, Jiménez-Sainz M, Fragoso R, Nazara Z, Cantu JM.
    Ann Genet; 1979 Jul; 22(3):155-7. PubMed ID: 316671
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  • 15. Tissue limited mosaicism in a patient with tetrasomy 9p.
    Papenhausen P, Riscile G, Miller K, Kousseff B, Tedesco T.
    Am J Med Genet; 1990 Nov; 37(3):388-91. PubMed ID: 2260570
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  • 17. An infant with trisomy 9pter yields 9q22 resulting from 3:1 segregation in a 46,XX t(1;9) (p36;q22) mother.
    Neu RL, Dennis NR, Lanman JT, Bannerman RM.
    Ann Genet; 1979 Nov; 22(3):151-4. PubMed ID: 316670
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  • 18. Isochromosome-formation in chromosome 9.
    Miller K, Arslan-Kirchner M.
    Ann Genet; 1994 Nov; 37(2):78-81. PubMed ID: 7985983
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  • 19. [Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father].
    Turleau C, De Grouchy J, Roubin M, Chavin-Colin F, Cachin O.
    Ann Genet; 1975 Jun; 18(2):125-9. PubMed ID: 1081365
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  • 20. Proximal interstitial deletion of 7q: a case report and review of the literature.
    Zackowski JL, Raffel LJ, Blank CA, Schwartz S.
    Am J Med Genet; 1990 Jul; 36(3):328-32. PubMed ID: 2194394
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