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Journal Abstract Search

190 related items for PubMed ID: 4639227

  • 1. An 18p21q translocation in a patient with presumptive "monosomy G".
    Cohen MM, Putnam TI.
    Am J Dis Child; 1972 Dec; 124(6):908-10. PubMed ID: 4639227
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  • 5. Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.
    Weber FM, Sparkes RS, Muller H.
    Cytogenetics; 1971 Dec; 10(6):404-12. PubMed ID: 5146417
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  • 9. Presumed disturbance of a nucleolus organizer in man: chromosome 13qs and monosomy 15 mosaicism.
    Hoehn H, Reinwein H.
    Humangenetik; 1971 Dec; 12(1):50-5. PubMed ID: 5556919
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  • 10. [Monosomy of chromosome 21].
    Rogóyski A, Babel M, Tronowska TD.
    Pediatr Pol; 1983 Jun; 58(6):557-9. PubMed ID: 6646915
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  • 11. Monosomy G: case report and review of the literature.
    Greenwood RD, Sommer A.
    J Med Genet; 1971 Dec; 8(4):496-500. PubMed ID: 5149533
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  • 14. Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).
    Reiss JA, Wyandt HE, Magenis RE, Lovrien EW, Hecht F.
    J Med Genet; 1972 Sep; 9(3):280-6. PubMed ID: 5079098
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  • 15. Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.
    Gustavson KH, Hitrec V, Santesson B.
    Clin Genet; 1972 Sep; 3(2):135-46. PubMed ID: 5054315
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  • 18. Monosomy 21: a possible stepwise evolution of the karyotype.
    Abeliovich D, Carmi R, Karplus M, Bar-Ziv J, Cohen MM.
    Am J Med Genet; 1979 Sep; 4(3):279-86. PubMed ID: 574719
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  • 19. An extra small metacentric chromosome in association with multiple congenital abnormalities.
    Finley WH, Finley SC, Monsky D.
    J Med Genet; 1971 Sep; 8(3):381-3. PubMed ID: 5097148
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  • 20. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
    Rivera H, Rivas F, Plascencia L, Cantú JM.
    Ann Genet; 1983 Sep; 26(4):234-7. PubMed ID: 6607704
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