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PUBMED FOR HANDHELDS

Journal Abstract Search


167 related items for PubMed ID: 4226082

  • 1. [Chromosome aberrations in Langdon-Down's disease].
    Mieler W.
    Dtsch Gesundheitsw; 1966 Feb 10; 21(6):263-9. PubMed ID: 4226082
    [No Abstract] [Full Text] [Related]

  • 2. [Genetic advice in Down's syndrome].
    Mikkelsen M.
    Nord Med; 1971 Apr 22; 85(16):515. PubMed ID: 4252403
    [No Abstract] [Full Text] [Related]

  • 3. [Cytogenetic study and chromosome abnormalities of Alzheimer's disease and Down's syndrome].
    Asaka A.
    Nihon Rinsho; 1988 Jul 22; 46(7):1502-7. PubMed ID: 2975715
    [No Abstract] [Full Text] [Related]

  • 4. Reproduction in down's syndrome (mongolism): chromosomal study of mother and normal child.
    Tagher P, Reisman LE.
    Obstet Gynecol; 1966 Feb 22; 27(2):182-4. PubMed ID: 4222376
    [No Abstract] [Full Text] [Related]

  • 5. [Dermatoglyphics in Down's syndrome. Comparison of results with those of an urban Mexican population].
    Armendares S, Del Castillo V, Cantú JM.
    Rev Invest Clin; 1972 Feb 22; 24(2):123-37. PubMed ID: 4262424
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  • 10. Chromosomal radiosensitivity in Down's syndrome.
    Sasaki MS, Tonomura A.
    Jinrui Idengaku Zasshi; 1969 Sep 22; 14(2):81-92. PubMed ID: 4244064
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  • 13. [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 Sep 22; 12(1):71-80. PubMed ID: 4235850
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  • 14. Familial D-D translocation. A family showing transmission through three generations; a case with multiple congenital malformations, and a case of regular 21-trisomic Down's syndrome.
    Visfeldt J.
    Acta Pathol Microbiol Scand; 1969 Sep 22; 75(4):545-54. PubMed ID: 4246134
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  • 16. [The semiological value of palmar prints of the hand in Down's syndrome].
    Galimberti A, Riggio G, Cardini G.
    Minerva Ortop; 1967 Oct 22; 18(10):607-10. PubMed ID: 4237838
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  • 17. [Oxygen consumption of leukocytes in chromosome abnormalities. (Down's syndrome, ring chromosome 21, cri-du-chat syndrome, trisomy 18 and 22)].
    Heyne K.
    Med Welt; 1980 Feb 15; 31(7):251-4. PubMed ID: 6445033
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