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Journal Abstract Search

129 related items for PubMed ID: 10658271

  • 1. [Karyological characteristics of Down's syndrome: clinical and theoretical aspects].
    Kovaleva NV, Butomo IV, Verlinskaia DK, Il'iashenko TN, Pantova IG, Prozorova MV, Khitrikova LE, Shandlorenko SK.
    Tsitologiia; 1999; 41(12):1014-21. PubMed ID: 10658271
    [Abstract] [Full Text] [Related]

  • 2. [Results of estimation of mutation rates for translocation trisomy 21].
    Kovaleva NV, Butomo IV, Il'iashenko TN, Vasil'eva IIu, Khitrikova LE, Shandlorenko SK, Prozorova MV.
    Tsitologiia; 2002; 44(11):1115-9. PubMed ID: 12561733
    [Abstract] [Full Text] [Related]

  • 3. 46,XX,t(15;21)/47,XX,15p-,+21 mosaicism in a child with Down's syndrome.
    Lucas J, Le Mee F, Pluquailec K, Le Marec B, Journel H, Picard F.
    Ann Genet; 1986; 29(2):104-6. PubMed ID: 2945509
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  • 4. Three interesting cases of Down's syndrome.
    Pérez-Castillo A, Del Mazo J, Abrisqueta JA.
    Ann Genet; 1983; 26(2):123-8. PubMed ID: 6225371
    [Abstract] [Full Text] [Related]

  • 5. Down's syndrome. I. Cytogenetics.
    Maximilian C, Duca D, Pop T, Toncescu N, Ioan D.
    Endocrinologie; 1980; 18(4):273-5. PubMed ID: 6451918
    [Abstract] [Full Text] [Related]

  • 6. Interchange trisomy 21 by t(1;21)(p22;q22)mat.
    Dominguez MG, Rivera H, Vasquez AI, Hernández-Zaragoza G, Rivas F.
    Genet Couns; 2001; 12(4):363-7. PubMed ID: 11837606
    [Abstract] [Full Text] [Related]

  • 7. [Sex ratio in Down syndrome].
    Kovaleva NV.
    Tsitol Genet; 2002; 36(6):54-69. PubMed ID: 12557485
    [Abstract] [Full Text] [Related]

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  • 9. Cytogenetic profile of Down syndrome in Alexandria, Egypt.
    Mokhtar MM, Abd el-Aziz AM, Nazmy NA, Mahrous HS.
    East Mediterr Health J; 2003; 9(1-2):37-44. PubMed ID: 15562731
    [Abstract] [Full Text] [Related]

  • 10. Unusual chromosome aberrations in 3 children with Down syndrome.
    Osztovics M, Tóth S, Wilhelm O.
    Acta Paediatr Acad Sci Hung; 1982; 23(3):283-9. PubMed ID: 6217717
    [Abstract] [Full Text] [Related]

  • 11. The future of prenatal diagnosis: rapid testing or full karyotype? An audit of chromosome abnormalities and pregnancy outcomes for women referred for Down's Syndrome testing.
    Ogilvie CM, Lashwood A, Chitty L, Waters JJ, Scriven PN, Flinter F.
    BJOG; 2005 Oct; 112(10):1369-75. PubMed ID: 16167939
    [Abstract] [Full Text] [Related]

  • 12. [Complete Down's syndrome in a boy, formed by chromosomic mosaicism 46-XY isochromosome 21 and 47-XY, trisomy 21 with mosaicism of the mother 46-XX and 47-XX, trisomy 21)].
    Raichs A, Tamparillas M.
    Sangre (Barc); 1967 Oct; 12(1):71-80. PubMed ID: 4235850
    [No Abstract] [Full Text] [Related]

  • 13. [Structural chromosomal reorganizations and mosaicism in the parents of children with Down's syndrome].
    Butomo IV, Kovaleva NV.
    Tsitol Genet; 1993 Oct; 27(1):87-91. PubMed ID: 8316960
    [Abstract] [Full Text] [Related]

  • 14. [Mutational level of translocated variants of Down's syndrome in Leningrad (1982-1991)].
    Kovaleva NV, Butomo IV, Verlinskaia DK, Mant DI, Pavlova MN, Pantova IG, Prozorova MV, Shandlorenko SK, Shmatova IA.
    Genetika; 1994 Mar; 30(3):428-32. PubMed ID: 8188060
    [Abstract] [Full Text] [Related]

  • 15. [Cytogenetic study of the parents of 85 index cases with regular trisomy 21].
    Armendares S, Buentello L, Salamanca F.
    Rev Invest Clin; 1990 Mar; 42(3):180-8. PubMed ID: 2148633
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  • 17. Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement.
    Tharapel AT, Redheendran R, Mankinen CB, Kukolich MK.
    J Med Genet; 1984 Oct; 21(5):391-5. PubMed ID: 6239037
    [Abstract] [Full Text] [Related]

  • 18. [Trisomy 21. Report of 2 cases with unusual karyotypes].
    Sánchez O, de Marade S, Guerra D.
    Invest Clin; 2001 Mar; 42(1):43-50. PubMed ID: 11294030
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  • 20. Cytogenetic investigations in cases of multiple developmental anomalies in children.
    Gajewska-Obel E, Gebala A, Rusin T, Rozynkowa O.
    Pol Med Sci Hist Bull (1973); 1975 Mar; 15(4):473-8. PubMed ID: 1223834
    [Abstract] [Full Text] [Related]

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