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Journal Abstract Search

146 related items for PubMed ID: 5146418

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  • 2. Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.
    Weber FM, Sparkes RS, Muller H.
    Cytogenetics; 1971; 10(6):404-12. PubMed ID: 5146417
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  • 4. 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. Inherited t(13q14q) in two retarded sisters.
    Crandall BF, Francke U, Campbell MA, Sparkes RS.
    Am J Hum Genet; 1972 Jul; 24(4):416-24. PubMed ID: 5031981
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  • 6. 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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  • 9. 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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  • 12. Presumed disturbance of a nucleolus organizer in man: chromosome 13qs and monosomy 15 mosaicism.
    Hoehn H, Reinwein H.
    Humangenetik; 1971 Sep; 12(1):50-5. PubMed ID: 5556919
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  • 13. A partial D-trisomy-normal mosaic female.
    Webb GC, Garson M, Robson MK, Pitt DB.
    J Med Genet; 1971 Dec; 8(4):522-7. PubMed ID: 5149538
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  • 15. Two human X-autosome translocations identified by autoradiography and fluorescence.
    Cohen MM, Lin CC, Sybert V, Orecchio EJ.
    Am J Hum Genet; 1972 Sep; 24(5):583-97. PubMed ID: 5054227
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  • 17. [A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].
    Bauchinger M, Schmid E, Röttinger E.
    Humangenetik; 1968 Sep; 6(4):303-10. PubMed ID: 5713616
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