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Journal Abstract Search

306 related items for PubMed ID: 604499

  • 21.
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  • 24. Trisomy 16q13----qter in a infant from a t(11;16)(q25;q13) translocation-carrier father.
    Hatanaka K, Ozaki M, Suzuki M, Murata R, Fujita H.
    Hum Genet; 1984; 65(3):311-5. PubMed ID: 6698553
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  • 25. [Trisomy 10 p. A previously reported case explained by binding].
    Turleau C, Doussau de Bazignan M, Roubin M, de Grouchy J.
    Ann Genet; 1976 Mar; 19(1):61-4. PubMed ID: 1084125
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  • 26. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG, Gracia R, López Pajares I, González M, Oliver A, Peralta A.
    An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
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  • 27. Partial trisomy of chromosome no. 1 in two adult brothers due to maternal translocation (1q--;6p+).
    Taysi K, Sekhon GS.
    Hum Genet; 1978 Nov 16; 44(3):277-85. PubMed ID: 730168
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  • 28. A malformed girl with duplication of chromosome 9q.
    Nakahori Y, Nakagome Y.
    J Med Genet; 1984 Oct 16; 21(5):387-8. PubMed ID: 6502654
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  • 29. Partial trisomy 9q resulting from a familial translocation t(9;16)(q32;q24).
    Soltan HC, Jung JH, Pyatt Z, Singh RP.
    Clin Genet; 1984 May 16; 25(5):449-54. PubMed ID: 6723106
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  • 30. The 2p partial trisomy syndrome. Duplication of region 2p23 leads to 2pter in two members of a t(2;7) translocation kindred.
    Francke U, Jones KL.
    Am J Dis Child; 1976 Nov 16; 130(11):1244-9. PubMed ID: 984008
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  • 33. Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.
    Mishra R, Paththinige CS, Sirisena ND, Nanayakkara S, Kariyawasam UGIU, Dissanayake VHW.
    BMC Pediatr; 2018 Jan 08; 18(1):4. PubMed ID: 29310616
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  • 35. Two children with partial trisomy for 7p.
    Berry AC, Honeycombe J, Macoun SJ.
    J Med Genet; 1979 Aug 08; 16(4):320-1. PubMed ID: 490588
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  • 36. A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defect.
    Orye E, Verhaaren H, Van Egmond H, Devloo-Blancquaert A.
    Clin Genet; 1975 Feb 08; 7(2):134-43. PubMed ID: 1132161
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  • 39. 47,XX,+der(18),t(9;18)(p24;q21) mat: a distinct partial trisomy 18q--syndrome?
    Bass HN, Weber-Parisi F, Sparkes RS.
    J Med Genet; 1978 Oct 08; 15(5):391-5. PubMed ID: 739531
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  • 40. Partial trisomy 13 as a result of de novo (6p;13q) translocation.
    Jones LA, Taysi K, Strauss AW, Hartmann AF.
    Hum Genet; 1979 Apr 27; 48(2):245-9. PubMed ID: 457146
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