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Journal Abstract Search

332 related items for PubMed ID: 422207

  • 1. 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).
    Fryns JP, Casaer P, Van den Berghe H.
    Hum Genet; 1979 Jan 25; 46(2):237-41. PubMed ID: 422207
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  • 2. 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 Jan 25; 32(3):177-9. PubMed ID: 2486064
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  • 3. Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/46,XX,r(22)/46,XX karyotype in the mother.
    Fryns JP, Van den Berghe H.
    Hum Genet; 1979 Mar 12; 47(2):213-6. PubMed ID: 437787
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  • 4. Mosaicism for trisomy 3q arising from an unbalanced, de novo t(3;15).
    Stallings R, Vaughn D, Hall K, Joyce C, Ryan F, Barton D, Geraghty M.
    J Med Genet; 1997 Jun 12; 34(6):512-4. PubMed ID: 9192276
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  • 5. Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother.
    Fujimoto A, Lin MS, Korula SR, Wilson MG.
    Am J Med Genet; 1985 Oct 12; 22(2):333-42. PubMed ID: 4050866
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  • 7. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.
    Verma RS, Dosik H, Wexler IB.
    J Genet Hum; 1977 Dec 12; 25(4):295-301. PubMed ID: 599332
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  • 8. Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother.
    Petković I, Barisić I, Bastić M, Hećimović S, Bago R.
    Am J Med Genet A; 2003 Jul 15; 120A(2):266-71. PubMed ID: 12833412
    [Abstract] [Full Text] [Related]

  • 9. 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.
    Brimblecombe FS, Lewis FJ, Vowles M.
    J Med Genet; 1977 Aug 15; 14(4):271-4. PubMed ID: 926139
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  • 10. Trisomy 10p due to a de novo t(10p;13p).
    Aller V, Abrisqueta JA, Pérez-Castillo A, del Mazo J, Martín-Lucas MA, de Torres ML.
    Hum Genet; 1979 Jan 25; 46(2):129-34. PubMed ID: 422195
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  • 11. Trisomy 20pter = to q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier mother.
    Schinzel A.
    Hum Genet; 1980 Feb 25; 53(2):169-72. PubMed ID: 7358383
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  • 15. Partial trisomy for the short arm of chromosome 2 due to familial balance translocation.
    Sekhon GS, Taysi K, Rath R.
    Hum Genet; 1978 Oct 19; 44(1):99-103. PubMed ID: 711241
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  • 16. Partial trisomy 11q as the result of sporadic translocation.
    Lurie IW, Lazjuk GI, Usova YI, Gurevich DB.
    Hum Genet; 1979 Sep 02; 51(1):63-6. PubMed ID: 500093
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  • 17. 19q distal trisomy due to a de novo (19;22)(q13.2;p11) translocation.
    Rivas F, García-Cruz D, Rivera H, Plascencia ML, González RM, Cantú JM.
    Ann Genet; 1985 Sep 02; 28(2):113-5. PubMed ID: 3876059
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  • 19. Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14)(p11;p11).
    Carnevale A, Frías S, del Castillo V.
    Clin Genet; 1978 Oct 02; 14(4):202-6. PubMed ID: 699358
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