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Journal Abstract Search

124 related items for PubMed ID: 1621764

  • 1. Reciprocal translocation t(1;15)(p36.2;p11.2): confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p).
    Barbi G, Kennerknecht I, Klett C.
    Am J Med Genet; 1992 Jul 01; 43(4):722-5. PubMed ID: 1621764
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  • 2. Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis.
    Blennow E, Bui TH, Wallin A, Kogner P.
    Am J Med Genet; 1996 Oct 02; 65(1):60-7. PubMed ID: 8914743
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  • 3. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.
    Wang JC, Nemana L, Kou SY, Habibian R, Hajianpour MJ.
    Am J Med Genet; 1997 Sep 05; 71(4):463-6. PubMed ID: 9286456
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  • 4. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
    Tharapel AT, Qumsiyeh MB, Martens PR, Tharapel SA, Dalton JD, Ward JC, Wilroy RS.
    Am J Med Genet; 1991 Jul 01; 40(1):117-20. PubMed ID: 1887840
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  • 5. Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.
    Gajecka M, Glotzbach CD, Jarmuz M, Ballif BC, Shaffer LG.
    Eur J Hum Genet; 2006 Dec 01; 14(12):1255-62. PubMed ID: 16941016
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  • 6. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
    Lestou VS, Ludkovski O, Connors JM, Gascoyne RD, Lam WL, Horsman DE.
    Genes Chromosomes Cancer; 2003 Apr 01; 36(4):375-81. PubMed ID: 12619161
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  • 7. Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.
    Alkan M, Ramelli GP, Hirsiger H, Keser I, Remonda L, Bühler EM, Moser H.
    Genet Couns; 2002 Apr 01; 13(2):151-6. PubMed ID: 12150215
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  • 8. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP, Devriendt K, Chern SR, Lee CC, Wang W, Lin SP.
    Prenat Diagn; 2000 May 01; 20(5):384-9. PubMed ID: 10820405
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  • 11. Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies.
    Courtens W, Petersen MB, Noël JC, Flament-Durand J, Van Regemorter N, Delneste D, Cochaux P, Verschraegen-Spae MR, Van Roy N, Speleman F.
    Am J Med Genet; 1994 Jul 01; 51(3):260-5. PubMed ID: 8074156
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  • 12. Cytogenetic and molecular studies of an X;21 translocation previously diagnosed as complete monosomy 21.
    Cardoso LC, Moraes L, Camilo MJ, Mulatinho MV, Ramos H, Almeida JC, Llerena JC, Seuánez HN, Vargas FR.
    Eur J Med Genet; 2008 Jul 01; 51(6):588-97. PubMed ID: 18674646
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  • 15. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
    Klein OD, Cotter PD, Albertson DG, Pinkel D, Tidyman WE, Moore MW, Rauen KA.
    Clin Genet; 2004 Jun 01; 65(6):477-82. PubMed ID: 15151506
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  • 16. Dissociation of tdic chromosomes: about a t(15;18)(p11;p11) leading to 18p monosomy.
    Garcia-Esquivel L, Rivera H, Sanchez-Corona J, Ramirez ML, Jimenez M, Cantú JM.
    Ann Genet; 1987 Jun 01; 30(2):94-7. PubMed ID: 3499849
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  • 17. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS, Hegmann K, Smith JL, Shaffer LG.
    Am J Med Genet; 1995 May 22; 57(1):31-4. PubMed ID: 7645595
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  • 18. Reassessment of two apparent deletions of chromosome 16p to an ins(11;16) and a t(1;16) by chromosome painting.
    Callen DF, Baker E, Eyre HJ, Chernos JE, Bell JA, Sutherland GR.
    Ann Genet; 1990 May 22; 33(4):219-21. PubMed ID: 2095703
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  • 19. Rearrangements of chromosome band 1p36 in non-Hodgkin's lymphoma.
    Dave BJ, Hess MM, Pickering DL, Zaleski DH, Pfeifer AL, Weisenburger DD, Armitage JO, Sanger WG.
    Clin Cancer Res; 1999 Jun 22; 5(6):1401-9. PubMed ID: 10389925
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  • 20. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Huang JK, Lee CC, Wang W.
    Genet Couns; 2006 Jun 22; 17(1):57-63. PubMed ID: 16719278
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