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Journal Abstract Search

480 related items for PubMed ID: 1472355

  • 1. Translocation/duplication of 9p onto a duplicated 4q.
    Rivera H, Figuera LE, Vasquez AI.
    Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
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  • 2. [Trisomy 5p due to paternal translocation (4;5) (q35;p12)].
    Menéndez I, Casaña H.
    Bol Med Hosp Infant Mex; 1993 Mar; 50(3):194-6. PubMed ID: 8442884
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  • 4. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA, Kamel AK, Ismail S, Helmy NA, Aglan MS, El Gammal M, El Ruby M, Mohamed AM.
    Genet Couns; 2007 Mar; 18(1):29-48. PubMed ID: 17515299
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  • 7. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS, Gibson L, McGrath J, Meyn MS, Breg WR, Yang-Feng TL.
    Am J Med Genet; 1993 May 15; 46(3):288-92. PubMed ID: 8488873
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  • 11. [Partial trisomy 11q 46, XX, 4q+ by translocation t (4; 11) (q35; q12)].
    Le Chevalier C, Chabrolle JP, Rossier A.
    Ann Pediatr (Paris); 1978 Nov 15; 25(9):501-4, 507. PubMed ID: 16114368
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  • 13. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
    Francisco-Bagnariolli AM, Payão SL, Kawasaki-Oyama RS, Sabbag Filho D, Segato R, de Labio RW, Chauffaille ML, Priest JH.
    Am J Med Genet; 2001 Nov 01; 103(4):302-7. PubMed ID: 11746010
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  • 14. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
    Ausems MG, Van Spijker HG, Dijkhuis HJ, Swanenburg De Veye HF, Bijlsma JB.
    Genet Couns; 1996 Nov 01; 7(1):61-5. PubMed ID: 8652090
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  • 15. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
    Merlob P, Kohn G, Litwin A, Nissenkorn I, Katznelson MB, Reisner SH.
    Am J Med Genet; 1989 Jan 01; 32(1):22-6. PubMed ID: 2705479
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  • 17. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
    Bhat M, Morrison PJ, Getty A, McManus D, Tubman R, Nevin NC.
    Am J Med Genet; 2000 Mar 20; 91(3):201-3. PubMed ID: 10756343
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  • 18. Duplication of distal 22q.
    Abeliovich D, Maor E, Bashan N, Carmi R.
    Am J Med Genet; 1989 Mar 20; 32(3):346-9. PubMed ID: 2729354
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  • 19. MCA/MR syndrome with features of Hallermann-Streiff syndrome and 4q deficiency/14q duplication.
    Fryns JP, Borghgraef M, Lemmens F, van den Berghe H.
    Clin Genet; 1993 Sep 20; 44(3):146-8. PubMed ID: 8275573
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