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PUBMED FOR HANDHELDS

Journal Abstract Search


276 related items for PubMed ID: 4279290

  • 1. Down's syndrome associated with two Robertsonian translocations, 45,XX,-15,-21, + t(15q21q) and 46,XX,-21, + t(21q21q).
    Atkins L, Bartsocas CS.
    J Med Genet; 1974 Sep; 11(3):306-9. PubMed ID: 4279290
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Karyotypic analysis of 150 cases of Down's Syndrome in Iraq.
    Ferman A, Shakir A.
    J Ment Defic Res; 1976 Jun; 20(2):83-7. PubMed ID: 133247
    [Abstract] [Full Text] [Related]

  • 4. An unusual case of mosaic Down's syndrome involving two different Robertsonian translocations.
    Clarke MJ, Thomson DA, Griffiths MJ, Bissenden JG, Aukett A, Watt JL.
    J Med Genet; 1989 Mar; 26(3):198-201. PubMed ID: 2523486
    [Abstract] [Full Text] [Related]

  • 5. t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndrome.
    Dallapiccola B, Bianco I, Brinchi V, Santulli B, Scarano G, Sicolo A, Stabile M, Ventruto V.
    Ann Genet; 1982 Mar; 25(1):56-8. PubMed ID: 6211124
    [Abstract] [Full Text] [Related]

  • 6. A case of atypical Down's syndrome with mosaic 46,XX/46,XX-21+t(21q21q).
    Hornstein L, Soukup S.
    Clin Genet; 1976 Aug; 10(2NA-NA-760903-760909):77-81. PubMed ID: 133775
    [No Abstract] [Full Text] [Related]

  • 7. De novo translocation Down's syndrome: risk of recurrence of Down's syndrome.
    Gardner RJ, Veale AM.
    Clin Genet; 1974 Aug; 6(3):160-4. PubMed ID: 4279152
    [No Abstract] [Full Text] [Related]

  • 8. Probable reciprocal translocation in somatic cells from patients with Down's syndrome.
    Sonta S, Oishi H.
    Jinrui Idengaku Zasshi; 1974 Sep; 19(2):169-73. PubMed ID: 4280457
    [No Abstract] [Full Text] [Related]

  • 9. 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 Sep; 29(2):104-6. PubMed ID: 2945509
    [Abstract] [Full Text] [Related]

  • 10. Structural chromosome abnormalities in Down syndrome: a study of two families.
    Jacobs PA, Mayer M, Rudak E.
    Cytogenet Cell Genet; 1978 Sep; 20(1-6):185-93. PubMed ID: 148351
    [Abstract] [Full Text] [Related]

  • 11. [Significance of chromosome translocations from the G-D group in the karyotype of the mother of 2 children with Down's syndrome].
    Dobrzańska A, Kostrzewski J.
    Pediatr Pol; 1970 Feb; 45(2):211-5. PubMed ID: 4245096
    [No Abstract] [Full Text] [Related]

  • 12. Human chromosome variation with two Robertsonian translocations.
    Morgan R, Bixenman H, Hecht F.
    Hum Genet; 1985 Feb; 69(2):178-80. PubMed ID: 3156085
    [Abstract] [Full Text] [Related]

  • 13. A familial tandem translocation (15;21) (q11;q22) in a case of Down's syndrome.
    Wahlström J, Djerg S.
    J Ment Defic Res; 1976 Sep; 20(3):171-8. PubMed ID: 135089
    [No Abstract] [Full Text] [Related]

  • 14. A case of mosaic Down's syndrome with two Robertsonian translocations.
    Leal-Garza CH, Cortés-Gutiérrez EI, Ortiz-Jalomo R, García-Cavazos R.
    Rev Invest Clin; 1996 Sep; 48(5):385-8. PubMed ID: 8968157
    [Abstract] [Full Text] [Related]

  • 15. Reciprocal translocation, 4q-; 21p+, giving rise to Down's syndrome.
    Jenkins MB, Boyd L.
    J Med Genet; 1976 Aug; 13(4):323-6. PubMed ID: 134161
    [Abstract] [Full Text] [Related]

  • 16. Down's syndrome. Incidence of translocations in Finland.
    Hongell K, Gripenberg U, Iivanainen M.
    Hum Hered; 1972 Aug; 22(1):7-14. PubMed ID: 4260911
    [No Abstract] [Full Text] [Related]

  • 17. Down's syndrome with 47,XX,+21-47,XX,+mar mosaicism.
    Weber FM, Sparkes RS, Muller H.
    J Med Genet; 1973 Jun; 10(2):177-9. PubMed ID: 4268391
    [Abstract] [Full Text] [Related]

  • 18. Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q).
    Vianna-Morgante AM, Nunesmaia HG.
    J Med Genet; 1978 Aug; 15(4):305-10. PubMed ID: 152355
    [Abstract] [Full Text] [Related]

  • 19. Unstable telocentric chromosome produced after centric misdivision of a 21q/21q translocated element.
    Guanti G, Maritato F.
    Hum Genet; 1978 Dec 29; 45(3):355-62. PubMed ID: 153887
    [Abstract] [Full Text] [Related]

  • 20. Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis.
    Caspersson T, Hultén M, Lindsten J, Therkelsen AJ, Zech L.
    Hereditas; 1971 Dec 29; 67(2):213-20. PubMed ID: 4142007
    [No Abstract] [Full Text] [Related]


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