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Journal Abstract Search

234 related items for PubMed ID: 8135272

  • 41. Familial t(4;13) with abnormal offspring in three generations.
    Najafzadeh TM, Littman VA, Dumars KW.
    Am J Med Genet; 1983 Sep; 16(1):15-22. PubMed ID: 6638065
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  • 42. Trisomy (12p) with telocentric and pseudoisodicentric chromosome formation in a fetus.
    Plaja A, Mediano C, Farran I, Vendrell T, Toran N, Gili T, Sanchez MA, Sarret E.
    Ann Genet; 1998 Sep; 41(1):52-5. PubMed ID: 9599652
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  • 47. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
    Rivera H, Rivas F, Plascencia L, Cantú JM.
    Ann Genet; 1983 Sep; 26(4):234-7. PubMed ID: 6607704
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  • 48. 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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  • 54. 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 May 15; 7(1):61-5. PubMed ID: 8652090
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  • 58. 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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  • 59. Brief clinical report: deletion of the long arm of chromosome 11, [del(11)(q23)].
    Monteleone PL, Chen SC, Nouri-Moghaddam S, Blair JD, Tietjens M.
    Am J Med Genet; 1982 Nov 15; 13(3):299-304. PubMed ID: 6891182
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  • 60. Emanuel syndrome due to unusual segregation of paternal origin.
    Zaki MS, Mohamed AM, Kamel AK, El-Gerzawy AM, El-Ruby MO.
    Genet Couns; 2012 Nov 15; 23(2):319-28. PubMed ID: 22876593
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