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Journal Abstract Search

143 related items for PubMed ID: 7927051

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  • 2. Partial trisomy 17q and monosomy 9p due to a familial translocation.
    Cotter PD, Stewart NL.
    Ann Genet; 1990; 33(4):231-3. PubMed ID: 1710432
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  • 6. Alternate, adjacent 2 and 3:1 meiotic segregation products from a balanced t(13;18) (q12;q11) carrier.
    Cotton C, Cummins M, Smith A.
    Clin Genet; 1993 Oct; 44(4):193-5. PubMed ID: 8261649
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  • 7. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
    Ausems MG, Van Spijker HG, Dijkhuis HJ, Swanenburg De Veye HF, Bijlsma JB.
    Genet Couns; 1996 Oct; 7(1):61-5. PubMed ID: 8652090
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  • 9. Partial trisomy 6p and partial monosomy 9p from a de novo translocation 46,XY, -9, +DER(9)T(6:9)(p211:p24).
    Eden MS, Thelin JW, Michalski K, Mitchell JA.
    Clin Genet; 1985 Nov; 28(5):375-84. PubMed ID: 4085142
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  • 11. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).
    van de Vooren MJ, Planteydt HT, Hagemeijer A, Peters-Slough MF, Timmerman MJ.
    Clin Genet; 1984 Jan; 25(1):52-8. PubMed ID: 6705241
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  • 12. Familial 4;18 chromosome translocation resulting in trisomy 4p and monosomy 18p: affected individuals with discordant phenotype.
    Berman DR, Couyoumjian CA, Treadwell MC, Barr M.
    Prenat Diagn; 2009 May; 29(5):538-40. PubMed ID: 19226522
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  • 13. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G, Jauch A, Eggermann T, Hardwick R, Kirsch S, Schiebel K, Rappold G, Robson L, Smith A.
    Am J Med Genet; 2000 May 15; 92(2):101-6. PubMed ID: 10797432
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  • 14. 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 May 15; 47(3):297-303. PubMed ID: 15337476
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  • 15. A child with partial trisomy of chromosome 17 and partial monosomy of chromosome 3: 46,XY,der(3),t(3;17)(p25;q23).
    Shawe DJ, Fear C, Appleyard WJ.
    J Med Genet; 1983 Oct 15; 20(5):383-5. PubMed ID: 6196484
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  • 16. Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).
    Brusnický J, van Heerden KM, de Jong G, Cronjé AS, Retief AE.
    J Med Genet; 1986 Oct 15; 23(5):435-45. PubMed ID: 3783620
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  • 17. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
    Akbas E, Polat S, Karakas-Celik S, Altintas ZM, Yildirim M, Yilgor E.
    Genet Couns; 2011 Oct 15; 22(4):417-23. PubMed ID: 22303803
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  • 18. Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus).
    Fonatsch C, Flatz SD.
    Humangenetik; 1974 Oct 15; 25(3):227-33. PubMed ID: 4141336
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  • 19. Distal trisomy of 10q with distal monosomy of 15q due to a paternal translocation.
    Sun SC, Luo FW, Song HW, He JB, Peng YS.
    J Int Med Res; 2009 Oct 15; 37(4):1230-7. PubMed ID: 19761709
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  • 20. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
    Balci S, Aypar E, Beksaç MS, Bartsch O.
    Genet Couns; 2009 Oct 15; 20(2):125-32. PubMed ID: 19650409
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