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Journal Abstract Search

254 related items for PubMed ID: 885143

  • 1. Tissue limited mosaicism for unbalanced autosomal translocation in a child with congenital anomalies and mental retardation.
    Summitt RL, Tharapel AT, Wilroy RS.
    Eur J Pediatr; 1977 Jul 01; 125(3):169-74. PubMed ID: 885143
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  • 4. 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).
    Fryns JP, Casaer P, Van den Berghe H.
    Hum Genet; 1979 Jan 25; 46(2):237-41. PubMed ID: 422207
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  • 5. Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation.
    Cantú ES, Thomas IT, Frias JL.
    Clin Genet; 1989 Sep 25; 36(3):189-95. PubMed ID: 2676269
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  • 8. 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 Sep 25; 5(3):188-95. PubMed ID: 4209591
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  • 9. Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues.
    Rudnik-Schöneborn S, Schubert R, Majewski F, Haverkamp F, Schwanitz G.
    Clin Genet; 1997 Aug 25; 52(2):126-9. PubMed ID: 9298749
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  • 12. Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother.
    Petković I, Barisić I, Bastić M, Hećimović S, Bago R.
    Am J Med Genet A; 2003 Jul 15; 120A(2):266-71. PubMed ID: 12833412
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  • 14. Mosaicism presumably related to a Y/6 translocation in a boy with multiple congenital abnormalities.
    Wisniewski L, Higgins JV.
    J Med Genet; 1977 Oct 15; 14(5):378-81. PubMed ID: 592355
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  • 15. Pallister-Killian syndrome in older children and adolescents.
    Horneff G, Majewski F, Hildebrand B, Voit T, Lenard HG.
    Pediatr Neurol; 1993 Oct 15; 9(4):312-5. PubMed ID: 8216546
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  • 17. Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis I.
    Petković I, de Capoa A, Giancotti P, Barisić I.
    Clin Genet; 1996 Dec 15; 50(6):515-9. PubMed ID: 9147886
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  • 18. Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.
    Kulharya AS, Lovell CM, Flannery DB.
    Am J Med Genet; 2002 Dec 15; 113(4):367-70. PubMed ID: 12457409
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  • 20. Mosaicism with a normal cell line and an unbalanced structural rearrangement.
    Zaslav AL, Fallet S, Blumenthal D, Jacob J, Fox J.
    Am J Med Genet; 1999 Jan 01; 82(1):15-9. PubMed ID: 9916836
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