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Journal Abstract Search

954 related items for PubMed ID: 4134631

  • 1. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J.
    Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
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  • 8. [Partial trisomy 11q;22q (author's transl)].
    Benítez J, Ayuso C, García Aparicio J, Sáez E, Pérez Sotelo A, Bello MJ.
    An Esp Pediatr; 1981 Sep; 15(3):293-300. PubMed ID: 7332142
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  • 9. Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.
    Podruch PE, Weisskopf B.
    J Pediatr; 1974 Jul; 85(1):92-5. PubMed ID: 4855265
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  • 10. Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.
    Lindenbaum RH, Bobrow M.
    J Med Genet; 1975 Mar; 12(1):29-43. PubMed ID: 123589
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  • 18. 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
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  • 19. Trisomy 9p resulting from maternal 9/21 translocation.
    Sŭbrt I, Blehová B, Pallová B.
    Hum Genet; 1976 May 19; 32(2):217-20. PubMed ID: 944684
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