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Journal Abstract Search

200 related items for PubMed ID: 422195

  • 21. Balanced translocation (10;13) in a father, ascertained through the study of meiosis in semen, and partial trisomy 10q in his son. Characterization of the region responsible for the partial trisomy 10q syndrome.
    Miró R, Templado C, Ponsá M, Serradell J, Marina S, Egozcue J.
    Hum Genet; 1980 Feb; 53(2):179-82. PubMed ID: 7358385
    [Abstract] [Full Text] [Related]

  • 22. Brother and sister with trisomy 10p. 46,XY,(22p+)mat; 46,XX,(22p+)mat.
    de Chieri P, Spatuzza E, Bonich JM.
    Hum Genet; 1978 Nov 24; 45(1):71-5. PubMed ID: 730183
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  • 25. Partial duplication of the short arm of chromosome 10. Karyotype: 46,XX,dup(10p)(pter to p12::p12::p12 to qter).
    Fryns JP, Deroover J, Haegeman J, Van den Berghe H.
    Hum Genet; 1979 Mar 12; 47(2):217-20. PubMed ID: 437788
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  • 26. Partial trisomy 12q: report of a case and review.
    Roberts SH, Mattina T, Laurence KM, Sorge G, Pavone L.
    J Med Genet; 1981 Dec 12; 18(6):470-3. PubMed ID: 7334509
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  • 27. Partial trisomy 7p in two families resulting from different balanced translocations.
    Moore CM, Pfeiffer RA, Craig-Holmes AP, Scott CI, Meisel-Stosiek M.
    Clin Genet; 1982 Feb 12; 21(2):112-21. PubMed ID: 7083611
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  • 29. 11q aneuploidy: partial monosomy and trisomy in the children of a mother with a t(3;11)(p27;q23) translocation.
    Ridler MA, McKeown JA.
    Hum Genet; 1979 Nov 01; 52(1):101-6. PubMed ID: 527970
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  • 30. Familial inversion translocation (8;13) with partial trisomy 13 in several family members.
    Pilgaard B, Jørgensen E, Knudsen VS, Mortensen E, Mikkelsen M.
    Eur J Pediatr; 1983 Apr 01; 140(2):105-8. PubMed ID: 6884384
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  • 32. Partial trisomy 12q24.31----qter.
    Tajara EH, Varella-Garcia M, Gusson AC.
    J Med Genet; 1985 Feb 01; 22(1):73-6. PubMed ID: 3981585
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  • 33. Trisomy 6qter.
    Turleau C, de Grouchy J.
    Clin Genet; 1981 Mar 01; 19(3):202-6. PubMed ID: 7273465
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  • 34. Trisomy 4p14 leads to 4pter with translocation t(4;15)(p14;p12) in the father.
    Schröchsnadel H, Feichtinger C, Scheminzky C.
    Humangenetik; 1975 Oct 07; 29(4):329-35. PubMed ID: 1176148
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  • 35. Paracentric Inversion in man: personal experience and review of the literature.
    Fryns JP, Van den Berghe H.
    Hum Genet; 1980 Oct 07; 54(3):413-6. PubMed ID: 7399530
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  • 37. Trisomy 9p in a patient with a de novo 9/15 translocation.
    Jacobsen P, Hobolth N, Mikkelsen M.
    Clin Genet; 1975 Apr 07; 7(4):317-24. PubMed ID: 1126053
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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 07; 15(5):391-5. PubMed ID: 739531
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