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PUBMED FOR HANDHELDS

Journal Abstract Search


185 related items for PubMed ID: 669713

  • 1.
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  • 2. The trisomy 8 syndrome: report of two further cases.
    Jacobsen P, Mikkelsen M, Rosleff F.
    Ann Genet; 1974 Jun; 17(2):87-94. PubMed ID: 4547945
    [No Abstract] [Full Text] [Related]

  • 3. Trisomy 9 mosaicism with multiple congenital anomalies.
    Haslam RH, Broske SP, Moore CM, Thomas GH, Neill CA.
    J Med Genet; 1973 Jun; 10(2):180-4. PubMed ID: 4714587
    [Abstract] [Full Text] [Related]

  • 4. Trisomy 8 mosaicism. A case report and a proposed list of the clinical features.
    Kosztolànyi G, Bühler EM, Elmiger P, Stalder GR.
    Eur J Pediatr; 1976 Nov 03; 123(4):293-300. PubMed ID: 991875
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  • 5. Trisomy 18 mosaicism: clues to the diagnosis.
    Bass HN, Fox M, Wulfsberg E, Sparkes RS, Crandall BF.
    Clin Genet; 1982 Dec 03; 22(6):327-30. PubMed ID: 7160104
    [Abstract] [Full Text] [Related]

  • 6. Dermatoglyphics in trisomy 8 mosaicism.
    Schaumann B.
    Humangenetik; 1974 Dec 03; 24(3):201-5. PubMed ID: 4442867
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  • 8. [Extreme tissue mosaicism in trisomy 8 syndrome. Trisomy 8 in fibroblasts and normal karyotype in lymphocytes].
    Meisel-Stosiek M, Pfeiffer RA, Tietze HU.
    Klin Padiatr; 1983 Dec 03; 195(5):365-8. PubMed ID: 6632718
    [Abstract] [Full Text] [Related]

  • 9. Presumptive mosaic partial trisomy associated with congenital anomalies and mental deficiency.
    Vianna-Morgante AM, Domingues WM, Ortega CC, Kasahara S.
    J Med Genet; 1974 Mar 03; 11(1):104-8. PubMed ID: 4134623
    [Abstract] [Full Text] [Related]

  • 10. Trisomy 12p syndrome: de novo occurrence of mosaic trisomy 12p in a mentally retarded boy.
    Kondo I, Hamaguchi H, Haneda T.
    Hum Genet; 1979 Jan 25; 46(2):135-40. PubMed ID: 422196
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  • 13. Chromosome aberrations in 50 patients with idiopathic mental retardation and in 50 control subjects. Madison blind study 3.
    Daly RF.
    J Pediatr; 1970 Sep 25; 77(3):444-53. PubMed ID: 5502094
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  • 15. 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 Sep 25; 55(1):31-8. PubMed ID: 7450754
    [Abstract] [Full Text] [Related]

  • 16. Trisomy 9 syndrome.
    Qazi QH, Masakawa A, Madahar C, Ehrlich R.
    Clin Genet; 1977 Oct 25; 12(4):221-6. PubMed ID: 912938
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