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Journal Abstract Search

156 related items for PubMed ID: 649151

  • 1. Partial monosomy 13 and 21 due to a familial 13/21 translocation.
    Otto PG, Toledo S, Richieri-Costa A, Otto PA, Vianna-Morgante AM, Kasahara S.
    Hum Genet; 1978 Apr 24; 41(3):243-50. PubMed ID: 649151
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  • 2. Unbalanced 13q/21q translocation: a revised study of the case previously reported as 21-monosomy.
    Ikeuchi T, Kondo I, Sasaki M, Kaneko Y, Kodama S.
    Hum Genet; 1976 Aug 30; 33(3):327-30. PubMed ID: 964993
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  • 4. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G, Forabosco A, Dutrillaux B.
    Ann Genet; 1974 Jun 30; 17(2):119-24. PubMed ID: 4547939
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  • 5. [Identification of 2 familial translocations].
    Laurent C, Biemont MC, Robert JM, Dutrillaux B.
    Ann Genet; 1974 Dec 30; 17(4):279-81. PubMed ID: 4548825
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  • 7. Familial tiny 9p/20p translocation: 9p24. The critical segment for monosomy 9p syndrome.
    Hoo JJ, Fischer A, Fuhrmann W.
    Ann Genet; 1982 Dec 30; 25(4):249-52. PubMed ID: 6985017
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  • 8. Inherited partial duplication of chromosome No. 15.
    Fujimoto A, Towner JW, Ebbin AJ, Kahlstrom EJ, Wilson MG.
    J Med Genet; 1974 Sep 30; 11(3):287-91. PubMed ID: 4139262
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  • 9. Partial trisomy 7p associated with familial 7p;22q translocation.
    Larson LM, Wasdahl WA, Jalal SM.
    J Med Genet; 1977 Aug 30; 14(4):258-61. PubMed ID: 926137
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  • 11. Banding identification of partial trisomy 15 and of 8/21 translocation.
    Wurster-Hill DH, Hoefnagel D.
    J Ment Defic Res; 1974 Jun 30; 18(2):139-44. PubMed ID: 4141377
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  • 16. A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.
    Valdmanis A, Pearson G, Siegel AE, Hoeksema RH, Mann JD.
    Ann Genet; 1967 Dec 30; 10(4):159-66. PubMed ID: 5301688
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  • 17. 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 30; 20(4):237-42. PubMed ID: 305749
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  • 18. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
    Howard-Peebles PN, Yarbrough KM, Stoddard GR, Rary JM.
    Clin Genet; 1977 Jan 30; 11(1):46-52. PubMed ID: 830449
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  • 19. [Monosomy 21 with mosaicism 45,XX,21--46,XX,21 pi].
    Emberger JM, Rey J, Rieu D, Dossa D, Bonnet H, Jean R.
    Arch Fr Pediatr; 1970 Jan 30; 27(10):1069-79. PubMed ID: 5495707
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