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Journal Abstract Search

123 related items for PubMed ID: 6616946

  • 21. Trisomy 10p produced by recombination involving maternal inversion inv(10)(pllq26).
    Lansky-Shafer SC, Daniel WL, Ruiz L.
    J Med Genet; 1981 Feb; 18(1):59-61. PubMed ID: 7253000
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  • 22. [Two new cases of trisomy 10q21 to 10qter in two sisters due to paternal translocation t(9;10) (q34;q24)].
    Fraisse J, Lauras B, La Selve A, Freycon F.
    Ann Genet; 1977 Jun; 20(2):128-31. PubMed ID: 302687
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  • 23. Partial 3q trisomy due to an unbalanced 3/10 translocation.
    Blumberg B, Moore R, Mohandas T.
    Am J Med Genet; 1980 Jun; 7(3):335-9. PubMed ID: 7468658
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  • 25. Partial trisomy 10p.
    Grosse KP, Schwanitz G, Singer H, Wieczorek V.
    Humangenetik; 1975 Sep 10; 29(2):141-4. PubMed ID: 1176136
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  • 26. Partial trisomy for the long arm of chromosome 7 due to familial balanced translocation.
    Schmid M, Wolf J, Nestler H, Krone W.
    Hum Genet; 1979 Jul 18; 49(3):283-9. PubMed ID: 478537
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  • 28. Partial 2p trisomy (p21 leads to pter) in two siblings of a family with a 2p-:15q+ translocation.
    Armendares S, Salamanca-Gómez F.
    Clin Genet; 1978 Jan 18; 13(1):17-24. PubMed ID: 624187
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  • 29. Distal 2q duplication: report of two familial cases and an attempt to define a syndrome.
    Zankl M, Schwanitz G, Schmid P, Zankl H, Dockter G, Rodewald A, Zang KD, Grosse KP.
    Am J Med Genet; 1979 Jan 18; 4(1):5-16. PubMed ID: 495653
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  • 30. 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.
    Brimblecombe FS, Lewis FJ, Vowles M.
    J Med Genet; 1977 Aug 18; 14(4):271-4. PubMed ID: 926139
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  • 33. Trisomy 10p due to t(5;10)(p15;p11) segregating in a large sibship.
    Back E, Vogel W, Hertel C, Schuchmann L.
    Hum Genet; 1978 Feb 23; 41(1):11-7. PubMed ID: 631856
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  • 37. Case report: partial trisomy 12p associated with 4p deletion due to paternal t(12p-;4p+) translocation.
    Carlin ME, Norman C.
    Birth Defects Orig Artic Ser; 1978 Feb 23; 14(6C):399-406. PubMed ID: 728595
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  • 38. Partial trisomy 14q due to familial t(14q-,11q+) translocation.
    Fryns JP, Van Eygen M, Tanghe W, Van Den Berghe H.
    Hum Genet; 1977 Jun 10; 37(1):105-10. PubMed ID: 881188
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