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Journal Abstract Search

198 related items for PubMed ID: 3735757

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  • 2. Analysis of banding patterns in a case of ring chromosome 21.
    Richer CL, Fitch N, Sitahal S, Murer-Orlando M, Jean P.
    Am J Med Genet; 1981; 10(4):323-31. PubMed ID: 7332027
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  • 5. A case of partial 9p monosomy with some unusual clinical features.
    Rutten FJ, Hustinx TW, Dunk-Tillemans AA, Scheres JM, Tjon YS.
    Ann Genet; 1978 Mar; 21(1):51-5. PubMed ID: 308344
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  • 6. [Two new cases of partial monosomy 11q with breakpoint in 11q24 (author's transl)].
    Laurent C, Biemont MC, Veyron M, Guilhot J, Guibaud P.
    Ann Genet; 1979 Mar; 22(4):239-41. PubMed ID: 317789
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  • 13. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
    Pai GS, Thomas GH, Leonard CO, Ward JC, Valle DL, Pyeritz RE.
    Johns Hopkins Med J; 1979 Oct; 145(4):162-9. PubMed ID: 491337
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  • 15. [Monosomy 21, G-deletion syndrome I, Anti-mongolism].
    Vestermark S, Mikkelsen M.
    Ugeskr Laeger; 1974 Aug 12; 136(33):1857. PubMed ID: 4280640
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  • 16. [De novo monosomy 4q32.1 leads to 4qter in a newborn with multiple malformations (author's transl)].
    Rethoré MO, Couturier J, Mselati JC, Cochois B, Lavaud J, Lejeune J.
    Ann Genet; 1979 Aug 12; 22(4):214-6. PubMed ID: 317783
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  • 18. Isochromosome-formation in chromosome 9.
    Miller K, Arslan-Kirchner M.
    Ann Genet; 1994 Aug 12; 37(2):78-81. PubMed ID: 7985983
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