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Journal Abstract Search

185 related items for PubMed ID: 669713

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  • 24. A woman with multiple congenital anomalies, mental retardation and mosaicism for an unusual translocation chromosome t(6;19).
    Pallister PD, Patau K, Inhorn SL, Opitz JM.
    Clin Genet; 1974; 5(3):188-95. PubMed ID: 4209591
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  • 25. Mixed sclerosing bone dysplasia, small stature, seizure disorder, and mental retardation: a syndrome?
    Jurenka SB, Van Allen MI.
    Am J Med Genet; 1995 May 22; 57(1):6-9. PubMed ID: 7645600
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  • 29. Three cases of trisomy 13 mosaicism and a review of the literature.
    Delatycki M, Gardner RJ.
    Clin Genet; 1997 Jun 22; 51(6):403-7. PubMed ID: 9237504
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  • 30. Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome.
    de France HF, Beemer FA, Senders RC, Schaminée-Main SC.
    Clin Genet; 1985 Jan 22; 27(1):92-6. PubMed ID: 3978842
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  • 33. Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.
    Allderdice PW, Miller OJ, Miller DA, Breg WR, Gendel E, Zelson C.
    Humangenetik; 1971 Jan 22; 13(3):205-9. PubMed ID: 5114675
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  • 35. 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 22; 30(5):433-5. PubMed ID: 8320712
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  • 37. Partial trisomy 12q24.31----qter.
    Tajara EH, Varella-Garcia M, Gusson AC.
    J Med Genet; 1985 Feb 22; 22(1):73-6. PubMed ID: 3981585
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