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Journal Abstract Search

270 related items for PubMed ID: 5713616

  • 1. [A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].
    Bauchinger M, Schmid E, Röttinger E.
    Humangenetik; 1968; 6(4):303-10. PubMed ID: 5713616
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  • 2. Presumed disturbance of a nucleolus organizer in man: chromosome 13qs and monosomy 15 mosaicism.
    Hoehn H, Reinwein H.
    Humangenetik; 1971; 12(1):50-5. PubMed ID: 5556919
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  • 5. 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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  • 8. Cytogenetic survey of 504 mentally retarded individuals.
    Singh DN, Osborne RA, Paul JR, Catoe S, Katzberg A, Hennigar GR, Barnett CD.
    J Ment Defic Res; 1974 Dec; 18(4):293-305. PubMed ID: 4282744
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  • 11. Frequency of chromosomal aberrations in newborn infants with multiple developmental defects.
    Chebotarev AN.
    Sov Genet; 1974 Sep 15; 8(10):1329-30. PubMed ID: 4439048
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  • 12. Trisomy/partial monosomy mosaicism of no. 13 pair [46, XX,--13, + rob(13q13q)/46, XX, r(13) (pllq34)].
    Oka S, Nakagome Y, Teramura F, Hosono F, Katumata M.
    Jinrui Idengaku Zasshi; 1977 Sep 15; 22(2-3):73-8. PubMed ID: 604564
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  • 13. "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 15; 26(4):234-7. PubMed ID: 6607704
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  • 14. Tandem duplication (5q13 to 22) in a mentally deficient girl.
    Kessel E, Pfeiffer RA.
    Hum Genet; 1979 Nov 15; 52(2):217-20. PubMed ID: 511177
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  • 15. Inv dup(15) supernumerary marker chromosomes.
    Webb T.
    J Med Genet; 1994 Aug 15; 31(8):585-94. PubMed ID: 7815414
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  • 18. Autosomal monosomy mosaicism in human bone marrow aspirate. Report of a case.
    Long DL, Pierre RV.
    Am J Clin Pathol; 1968 Oct 15; 50(4):482-4. PubMed ID: 5676342
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