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Journal Abstract Search

168 related items for PubMed ID: 2793173

  • 41. The translocation 11q;22q: a novel unbalanced karyotype.
    Abeliovich D, Carmi R.
    Am J Med Genet; 1990 Oct; 37(2):288. PubMed ID: 2248300
    [No Abstract] [Full Text] [Related]

  • 42. Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(11;22)(q23;q11).
    Martin RH.
    Clin Genet; 1984 Apr; 25(4):357-61. PubMed ID: 6713713
    [Abstract] [Full Text] [Related]

  • 43. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J, Chernos J, Roland B.
    Am J Med Genet; 1997 Dec 19; 73(3):327-9. PubMed ID: 9415693
    [Abstract] [Full Text] [Related]

  • 44. Unbalanced translocation 46,XY,-15,+der(22)t(15;22)(q13;q11)pat: case report and review of the literature.
    Van Hove JL, McConkie-Rosell A, Chen YT, Iafolla AK, Lanman JT, Hennessy MD, Kahler SG.
    Am J Med Genet; 1992 Sep 01; 44(1):24-30. PubMed ID: 1519645
    [Abstract] [Full Text] [Related]

  • 45. Lack of intraindividual variation of unbalanced spermatozoa frequencies from a 46,XY,t(9;22)(q21;q11.2) carrier: case report.
    Morel F, Douet-Guilbert N, Le Bris MJ, Herry A, Marchetti C, Lefebvre V, Delobel B, Amice V, Amice J, De Braekeleer M.
    Hum Reprod; 2004 Oct 01; 19(10):2227-30. PubMed ID: 15298974
    [Abstract] [Full Text] [Related]

  • 46. Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22).
    Balci S, Engiz O, Yilmaz Z, Baltaci V.
    Genet Couns; 2006 Oct 01; 17(3):281-9. PubMed ID: 17100195
    [Abstract] [Full Text] [Related]

  • 47. Specific subtelomere loss on chromosome der(11)t(3;11)(q23;q23)x2 in anaplastic thyroid cancer cell line OCUT-1.
    Kammori M, Onoda N, Nakamura K, Izumiyama N, Ogisawa K, Kurabayashi R, Ogawa T, Kaminishi M, Poon SS, Takubo K.
    Int J Mol Med; 2006 Jul 01; 18(1):9-16. PubMed ID: 16786150
    [Abstract] [Full Text] [Related]

  • 48. Translocation t(1;22) mimicking t(1;19) in a child with acute lymphoblastic leukemia as revealed by chromosome painting.
    Rieder H, Kolbus U, Koop U, Ludwig WD, Stollmann-Gibbels B, Fonatsch C.
    Leukemia; 1993 Oct 01; 7(10):1663-6. PubMed ID: 8412330
    [Abstract] [Full Text] [Related]

  • 49. Recurrent adjacent-2 segregation of a familial t(14;21)(q11.2;q11.2): phenotypic comparison of two brothers and a paternal aunt inheriting the der(14).
    Chen E, Choe MA, Loughman WD, Covert S, Bitts S, Rowe A, Beischel L, Johnson JP.
    Am J Med Genet A; 2005 Jan 15; 132A(2):164-70. PubMed ID: 15551340
    [Abstract] [Full Text] [Related]

  • 50. Maternal translocation (9;18) with two abnormal offspring each with different chromosome derivatives.
    Pearson M, Riske C, Allanson JE.
    J Med Genet; 1989 Oct 15; 26(10):655-8. PubMed ID: 2585464
    [Abstract] [Full Text] [Related]

  • 51. Molecular cytogenetic analysis discloses complex genetic imbalance in a t(11;21) myelodysplastic syndrome.
    Kerim S, Rege-Cambrin G, Guerrasio A, Rosso C, Van Den Berghe H.
    Cancer Genet Cytogenet; 1990 Jun 15; 46(2):243-50. PubMed ID: 2187596
    [Abstract] [Full Text] [Related]

  • 52. Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridization.
    Levy B, Gershin IF, Desnick RJ, Babu A, Gelb BD, Hirschhorn K, Cotter PD.
    Cytogenet Cell Genet; 1997 Jun 15; 76(1-2):68-71. PubMed ID: 9154131
    [Abstract] [Full Text] [Related]

  • 53. Duplication of distal 22q.
    Abeliovich D, Maor E, Bashan N, Carmi R.
    Am J Med Genet; 1989 Mar 15; 32(3):346-9. PubMed ID: 2729354
    [Abstract] [Full Text] [Related]

  • 54. Translocation t(11;22)(q23;q11) in an adult with acute monoblastic leukemia.
    Kobayashi H, Miyachi H, Ogawa T, Jimbo M.
    Jpn J Med; 1990 Mar 15; 29(5):527-32. PubMed ID: 2089178
    [Abstract] [Full Text] [Related]

  • 55. Familial interstitial duplication of 11q; partial trisomy (11)(q13.5q21).
    Yelavarthi KK, Zunich J.
    Am J Med Genet A; 2004 May 01; 126A(4):423-6. PubMed ID: 15098242
    [Abstract] [Full Text] [Related]

  • 56. Reproductive risk in mating between two translocation carriers: case report and review of the literature.
    Tsuji K, Narahara K, Yokoyama Y, Ninomiya S, Yonesawa S, Hiramatsu Y, Masaoka H, Kudo N, Seino Y.
    Am J Med Genet; 1993 Jun 15; 46(5):524-8. PubMed ID: 8322814
    [Abstract] [Full Text] [Related]

  • 57. Subfertile couple with t(4;22)(q23;q11.2).
    Srebniak M, Popowska L, Wawrzkiewicz-Witkowska A, Tomaszewska A, Kazmierczak W.
    J Appl Genet; 2005 Jun 15; 46(3):333-6. PubMed ID: 16110194
    [Abstract] [Full Text] [Related]

  • 58. Renal cell carcinoma and a constitutional t(11;22)(q23;q11.2): case report and review of the potential link between the constitutional t(11;22) and cancer.
    Doyen J, Carpentier X, Haudebourg J, Hoch B, Karmous-Benailly H, Ambrosetti D, Fabas T, Amiel J, Lambert JC, Pedeutour F.
    Cancer Genet; 2012 Nov 15; 205(11):603-7. PubMed ID: 23117075
    [Abstract] [Full Text] [Related]

  • 59. A case with Emanuel syndrome: extra derivative 22 chromosome inherited from the mother.
    İkbal Atli E, Gürkan H, Vatansever Ü, Ulusal S, Tozkir H.
    Balkan J Med Genet; 2015 Dec 01; 18(2):77-82. PubMed ID: 27785401
    [Abstract] [Full Text] [Related]

  • 60. Analysis of meiotic segregation in a man heterozygous for two reciprocal translocations using the hamster in vitro penetration system.
    Burns JP, Koduru PR, Alonso ML, Chaganti RS.
    Am J Hum Genet; 1986 Jun 01; 38(6):954-64. PubMed ID: 3728467
    [Abstract] [Full Text] [Related]

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