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Journal Abstract Search

239 related items for PubMed ID: 3621653

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  • 5. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M, Mutoh K, Okuno T, Mikawa H, Edagawa J, Abe T.
    Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486
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  • 6. Trisomy 9 mosaicism with multiple congenital anomalies.
    Haslam RH, Broske SP, Moore CM, Thomas GH, Neill CA.
    J Med Genet; 1973 Jun; 10(2):180-4. PubMed ID: 4714587
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  • 8. Trisomy 9 mosaicism in two girls with multiple congenital malformations and mental retardation.
    Stoll C, Chognot D, Halb A, Luckel JC.
    J Med Genet; 1993 May; 30(5):433-5. PubMed ID: 8320712
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  • 13. Interstitial duplication of 7(q22-->q34).
    Stratton RF, DuPont BR, Mattern VL, Schelonka RL, Moore CM.
    Am J Med Genet; 1993 Sep 01; 47(3):380-2. PubMed ID: 8135285
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  • 14. Pure duplication 1q41-qter: further delineation of trisomy 1q syndromes.
    Kulikowski LD, Bellucco FT, Nogueira SI, Christofolini DM, Smith Mde A, de Mello CB, Brunoni D, Melaragno MI.
    Am J Med Genet A; 2008 Oct 15; 146A(20):2663-7. PubMed ID: 18798309
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  • 15. Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18.
    Boghosian-Sell L, Mewar R, Harrison W, Shapiro RM, Zackai EH, Carey J, Davis-Keppen L, Hudgins L, Overhauser J.
    Am J Hum Genet; 1994 Sep 15; 55(3):476-83. PubMed ID: 8079991
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  • 17. New chromosomal syndromes.
    Lewandowski RC, Yunis JJ.
    Am J Dis Child; 1975 Apr 15; 129(4):515-29. PubMed ID: 124130
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  • 18. Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the risk.
    Stengel-Rutkowski S, Lohse K, Herzog C, Apacik C, Couturier J, Albert A, Belohradsky B.
    Clin Genet; 1992 Oct 15; 42(4):178-85. PubMed ID: 1424241
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  • 19. Three cases of 16q duplication.
    Maher ER, Willatt L, Cuthbert G, Chapman C, Hodgson SV.
    J Med Genet; 1991 Nov 15; 28(11):801-2. PubMed ID: 1820771
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  • 20. Uniparental isodisomy due to duplication of chromosome 21 occurring in somatic cells monosomic for chromosome 21.
    Petersen MB, Bartsch O, Adelsberger PA, Mikkelsen M, Schwinger E, Antonarakis SE.
    Genomics; 1992 Jun 15; 13(2):269-74. PubMed ID: 1351865
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