BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 18758173)

  • 1. A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences.
    Mrasek K; Krüger G; Bauer I; Müller-Navia J; Liehr T; Weise A
    Cytogenet Genome Res; 2008; 121(3-4):286-7. PubMed ID: 18758173
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
    Wyandt HE; Shim SH; Mark HF; Huang XL; Milunsky JM
    Exp Mol Pathol; 2006 Jun; 80(3):262-6. PubMed ID: 16516886
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.
    Liehr T; Stumm M; Wegner RD; Bhatt S; Hickmann P; Patsalis PC; Meins M; Morlot S; Klaschka V; Ewers E; Hinreiner S; Mrasek K; Kosyakova N; Cai WW; Cheung SW; Weise A
    Cytogenet Genome Res; 2009; 124(1):102-5. PubMed ID: 19372675
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 36(4):375-81. PubMed ID: 12619161
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recurrent duplication of Xq27-qter in hematological malignancies revealed by multicolor fluorescence in situ hybridization and multicolor banding.
    MacKinnon RN; Zordan A; Campbell LJ
    Cancer Genet Cytogenet; 2005 Sep; 161(2):125-9. PubMed ID: 16102582
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Duplication of chromosome region 8p23.1-->p23.3: a benign variant?
    Engelen JJ; Moog U; Evers JL; Dassen H; Albrechts JC; Hamers AJ
    Am J Med Genet; 2000 Mar; 91(1):18-21. PubMed ID: 10751083
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Analysis of a case of balanced chromosome translocation and phenotypic abnormality by fluorescence in situ hybridization].
    Zhu G; Bartsch O; Wan M; Gillessen-Kaesbach G; Passarge E
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr; 18(2):96-9. PubMed ID: 11295125
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Delimitation of duplicated segments and identification of their parental origin in two partial chromosome 3p duplications.
    Antonini S; Kim CA; Sugayama SM; Vianna-Morgante AM
    Am J Med Genet; 2002 Nov; 113(2):144-50. PubMed ID: 12407704
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Is there a yet unreported unbalanced chromosomal abnormality without phenotypic consequences in proximal 4p?
    Liehr T; Bartels I; Zoll B; Ewers E; Mrasek K; Kosyakova N; Merkas M; Hamid AB; von Eggeling F; Posorski N; Weise A
    Cytogenet Genome Res; 2011; 132(1-2):121-3. PubMed ID: 20639618
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of recurrent chromosomal breakpoints in multiple myeloma with complex karyotypes by combined G-banding, spectral karyotyping, and fluorescence in situ hybridization analyses.
    Sáez B; Martín-Subero JI; Largo C; Martín MC; Odero MD; Prosper F; Siebert R; Calasanz MJ; Cigudosa JC
    Cancer Genet Cytogenet; 2006 Sep; 169(2):143-9. PubMed ID: 16938572
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.
    Di Giacomo MC; Cesarano C; Bukvic N; Manisali E; Guanti G; Susca F
    Prenat Diagn; 2004 Aug; 24(8):619-22. PubMed ID: 15305349
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.
    Bartels I; Starke H; Argyriou L; Sauter SM; Zoll B; Liehr T
    Eur J Med Genet; 2007; 50(2):133-8. PubMed ID: 17174164
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Boy with an interstitial 1q (q31q41) duplication confirmed by fluorescent in situ hybridisation.
    Sillén A; Wadelius C; Annerén G
    Am J Med Genet; 1998 Nov; 80(2):163-8. PubMed ID: 9805135
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Direct duplication of 9p22-->p24 in a child with duplication 9p syndrome.
    Fujimoto A; Lin MS; Schwartz S
    Am J Med Genet; 1998 May; 77(4):268-71. PubMed ID: 9600733
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial duplication of 3q (q25.1-->q26.1) without the Brachmann-de Lange phenotype.
    Lopez-Rangel E; Dill FJ; Hrynchak MA; Van Allen MI
    Am J Med Genet; 1993 Nov; 47(7):1068-71. PubMed ID: 8291525
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers.
    Arens YH; Engelen JJ; Govaerts LC; van Ravenswaay CM; Loneus WH; van Lent-Albrechts JC; van der Blij-Philipsen M; Hamers AJ; Schrander-Stumpel CT
    Am J Med Genet A; 2004 Oct; 130A(2):128-33. PubMed ID: 15372532
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromosome 1 abnormalities in multiple myeloma.
    Marzin Y; Jamet D; Douet-Guilbert N; Morel F; Le Bris MJ; Morice P; Abgrall JF; Berthou C; De Braekeleer M
    Anticancer Res; 2006; 26(2A):953-9. PubMed ID: 16619492
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A familial inverted duplication 2q33-q34 identified and delineated by multiple cytogenetic techniques.
    Eussen BH; van de Laar I; Douben H; van Kempen L; Hochstenbach R; De Man SA; Van Opstal D; de Klein A; Poddighe PJ
    Eur J Med Genet; 2007; 50(2):112-9. PubMed ID: 17161033
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variant.
    Lukusa T; Devriendt K; Holvoet M; Fryns JP
    Am J Med Genet; 2000 Mar; 91(3):192-7. PubMed ID: 10756341
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Investigation of bone marrow involvement in malignant lymphoma using fluorescence in situ hybridization: possible utility in the detection of micrometastasis.
    Huh HJ; Min HC; Cho HI; Chae SL; Lee DS
    Cancer Genet Cytogenet; 2008 Oct; 186(1):1-5. PubMed ID: 18786435
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.