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Journal Abstract Search

143 related items for PubMed ID: 596115

  • 1.
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  • 2. A complex mosaic with D/E translocation tdic(15;18) (p12;p11) in an oligospermic male with apparently total infertility.
    Singh-Kahlon DP, Serra A, Bova R.
    Clin Genet; 1977 May; 11(5):342-8. PubMed ID: 862211
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  • 5. Trisomy 8. Report of a mosaic human male with near-normal phenotype and normal IQ, ascertained through infertility.
    Chandley AC, Hargreave TB, Fletcher JM, Soos M, Axworthy D, Price WH.
    Hum Genet; 1980 May; 55(1):31-8. PubMed ID: 7450754
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  • 7. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY.
    Am J Med Genet; 1994 Nov 01; 53(2):108-40. PubMed ID: 7856637
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  • 9. Cytogenetic results from the U.S. Collaborative Study on CVS.
    Ledbetter DH, Zachary JM, Simpson JL, Golbus MS, Pergament E, Jackson L, Mahoney MJ, Desnick RJ, Schulman J, Copeland KL.
    Prenat Diagn; 1992 May 01; 12(5):317-45. PubMed ID: 1523201
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  • 10. Chromosomal constitution of infertile men.
    Mićić M, Mićić S, Diklić V.
    Clin Genet; 1984 Jan 01; 25(1):33-6. PubMed ID: 6705240
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  • 11. [Clinical and cytogenetic observations on 2 mosaic C trisomic adults. Individualization of the supernumerary chromosome with the modern denaturation technic: 47, XY, ?8 +].
    Laurent C, Robert JM, Grambert J, Dutrillaux B.
    Lyon Med; 1971 Dec 26; 226(20):827-33. PubMed ID: 5144392
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  • 13. Increased aneuploidy rates in spermatozoa of a male carrier of a trisomy 18 mosaicism.
    Perrin A, Douet-Guilbert N, Le Bris MJ, May-Panloup P, Guichet A, Amice V, Amice J, De Braekeleer M, Morel F.
    Int J Androl; 2009 Jun 26; 32(3):231-4. PubMed ID: 18217987
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  • 14. Cri du chat-syndrome in combination with partial trisomy 9 p.
    Sigmund J, Frisch H, Heinz-Erian P, Rhomberg K, Wegner RD.
    Padiatr Padol; 1986 Jun 26; 21(1):61-7. PubMed ID: 3960564
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  • 15. Autosomal chromosome disorders and variations.
    Miller OJ, Breg WR.
    N Engl J Med; 1976 Mar 11; 294(11):596-8. PubMed ID: 1246243
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  • 16. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.
    Schinzel A, Kotzot D, Brecevic L, Robinson WP, Dutly F, Dauwerse H, Binkert F, Baumer A, Ausserer B.
    Eur J Hum Genet; 1997 Mar 11; 5(5):308-14. PubMed ID: 9412788
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  • 17. Three unusual trisomic patterns in children. Triple X plus triple E-triple X mosaic: normal XY-D trisomy mosaic; partial trisomy with E translocation.
    Engel E, Haddow JE, Lewis JF, Tipton RE, Overall JC, McGee BJ, Levrat OJ, Engel-de-montmollin M.
    Am J Dis Child; 1967 Mar 11; 113(3):322-8. PubMed ID: 6019450
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  • 18. Acute leukemia associated with trisomy 8 mosaicism and a familial translocation 46,XY,t(7;20)(p13;p12).
    Riccardi VM, Humbert JR, Peakman D.
    Am J Med Genet; 1978 Mar 11; 2(1):15-21. PubMed ID: 299456
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  • 19. Mosaicism presumably related to a Y/6 translocation in a boy with multiple congenital abnormalities.
    Wisniewski L, Higgins JV.
    J Med Genet; 1977 Oct 11; 14(5):378-81. PubMed ID: 592355
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  • 20. [Frequency of mixoploidy in 85 index cases with Down syndrome].
    Armendares S, Buentellos L, Salamanca F.
    Rev Invest Clin; 1990 Oct 11; 42(2):103-7. PubMed ID: 2148432
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