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Journal Abstract Search

170 related items for PubMed ID: 1081364

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  • 6. Presumably balanced translocations involving the same band of chromosome No. 4 found in two mentally retarded, dysmorphic individuals.
    Skovby F, Niebuhr E.
    Ann Genet; 1974 Dec; 17(4):243-9. PubMed ID: 4141591
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  • 8. De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy.
    Fryns JP, Kleczkowska A, Kenis H.
    Ann Genet; 1984 Dec; 27(1):62-4. PubMed ID: 6609678
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  • 11. De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.
    Chitayat D, Fagerstrom CL, Kalousek DK, Rootman J, Taylor GP, Hall JG.
    Am J Med Genet; 1989 Jan; 32(1):36-41. PubMed ID: 2495721
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  • 12. [Partial trisomy 15q due to maternal translocation t(7;15)(q35;14)].
    Castel Y, Rivière D, Boycly JY, Toudic L.
    Ann Genet; 1976 Mar; 19(1):15-9. PubMed ID: 1084116
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  • 13. A mentally and physically retarded girl with a familial balanced reciprocal translocation t(7;13).
    Knuutila S, Panelius M, Pihlaja T.
    Hereditas; 1977 Mar; 85(2):249-50. PubMed ID: 885733
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  • 15. Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family.
    Wilroy RS, Summitt RL, Martens P, Gooch WM.
    Ann Genet; 1977 Dec; 20(4):237-42. PubMed ID: 305749
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  • 16. Brief clinical report: dup(4p15 leads to 4pter) in a 19-year-old woman resulting from a maternal 4;14 translocation.
    Clark CE, Telfer MA, Cowell HR, Kalamchi A, Steg NL.
    Am J Med Genet; 1982 Jan; 11(1):37-42. PubMed ID: 7065001
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  • 17. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP, Kleczkowska A, Jaeken J, Van Herck K, Van den Berghe MH.
    Ann Genet; 1989 Jan; 32(3):177-9. PubMed ID: 2486064
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  • 18. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
    Legare JM, Sekhon GS, Laxova R.
    Am J Med Genet; 1994 Nov 15; 53(3):216-21. PubMed ID: 7856655
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  • 19. Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).
    Fryns JP, Kleczkowska A, Smeets E, Thiry P, Geutjens J, Van den Berghe H.
    Am J Med Genet; 1990 Dec 15; 37(4):546-7. PubMed ID: 2260606
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  • 20. [The clinical picture of 13q22-qter duplication in a 2-year-old boy].
    Halasová E, Lukácová M, Bergendiová E, Kamenická E.
    Cesk Pediatr; 1987 Aug 15; 42(8):477-9. PubMed ID: 3664759
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