BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

90 related articles for article (PubMed ID: 16259332)

  • 21. Concurrent acute myeloid leukemia with inv(16)(p13.1q22) and chronic lymphocytic leukemia: molecular evidence of two separate diseases.
    Lu CM; Murata-Collins JL; Wang E; Siddiqi I; Lawrence H
    Am J Hematol; 2006 Dec; 81(12):963-8. PubMed ID: 16917916
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Trisomy 22 as the sole abnormality is an important marker for the diagnosis of acute myeloid leukemia with inversion 16.
    Xu W; Zhou HF; Fan L; Qian SX; Chen LJ; Qiu HR; Zhang SJ; Li JY
    Onkologie; 2008 Sep; 31(8-9):440-4. PubMed ID: 18787351
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Xp11 translocation renal cell carcinoma in adults: expanded clinical, pathologic, and genetic spectrum.
    Argani P; Olgac S; Tickoo SK; Goldfischer M; Moch H; Chan DY; Eble JN; Bonsib SM; Jimeno M; Lloreta J; Billis A; Hicks J; De Marzo AM; Reuter VE; Ladanyi M
    Am J Surg Pathol; 2007 Aug; 31(8):1149-60. PubMed ID: 17667536
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Premature ovarian failure in a patient with a complex chromosome rearrangement involving the critical region Xq24, characterized by analysis using fluorescence in situ hybridization by chromosome microdissection.
    Weimer J; Shivakumar S; Danda S; Thomas N; Ralui LP; Jonat W; Arnold N
    Fertil Steril; 2007 Dec; 88(6):1677.e9-13. PubMed ID: 17482166
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The 10-Mb paracentric inversion of chromosome arm 2p in activating MSH2 and causing hereditary nonpolyposis colorectal cancer: re-annotation and mutational mechanisms.
    Chen JM
    Genes Chromosomes Cancer; 2008 Jun; 47(6):543-5. PubMed ID: 18335504
    [No Abstract]   [Full Text] [Related]  

  • 26. [Genetic analysis of a complex chromosome rearrangement involving two chromosomes and four breakpoints in an azoospermic man].
    Luo YQ; Shen M; Qian YL; Chen YL; Xu CM; Jin F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):200-2. PubMed ID: 19350516
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm.
    Bhatt S; Moradkhani K; Mrasek K; Puechberty J; Lefort G; Lespinasse J; Sarda P; Liehr T; Hamamah S; Pellestor F
    Mol Hum Reprod; 2007 Oct; 13(10):751-6. PubMed ID: 17913851
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome.
    Wimplinger I; Rauch A; Orth U; Schwarzer U; Trautmann U; Kutsche K
    Eur J Med Genet; 2007; 50(6):421-31. PubMed ID: 17845869
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel t(2;3)(p11;q27) in a case of follicular lymphoma.
    Tapinassi C; Micucci C; Lahortiga I; Malazzi O; Gasparini P; Gorosquieta A; Odero MD; Belloni E
    Cancer Genet Cytogenet; 2007 Jan; 172(1):70-3. PubMed ID: 17175383
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia.
    de Jesus Marques-Salles T; Liehr T; Mkrtchyan H; Raimondi SC; Tavares de Souza M; de Figueiredo AF; Rouxinol S; Jordy Macedo FC; Abdelhay E; Santos N; Macedo Silva ML
    Cancer Genet Cytogenet; 2009 Feb; 189(1):59-62. PubMed ID: 19167614
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [A rare tumour of the arm in a child].
    Boujelbène N; Chadli-Debbiche A; Chèrif K; Kilani H; Labbène N; Khayat O; Kaâbar N; Saied S; Ben Ayed M
    Ann Pathol; 2009 Feb; 29(1):44-6. PubMed ID: 19233095
    [No Abstract]   [Full Text] [Related]  

  • 32. Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.
    Liehr T; Mrasek K; Hinreiner S; Reich D; Ewers E; Bartels I; Seidel J; Emmanuil N; Petesen M; Polityko A; Dufke A; Iourov I; Trifonov V; Vermeesch J; Weise A
    Sex Dev; 2007; 1(6):353-62. PubMed ID: 18391547
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Translocations t(X;14)(q28;q11) and t(Y;14)(q12;q11) in T-cell prolymphocytic leukemia.
    de Oliveira FM; Tone LG; Simões BP; Rego EM; Marinato AF; Jácomo RH; Falcão RP
    Int J Lab Hematol; 2009 Aug; 31(4):453-6. PubMed ID: 18294235
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Paracentric inversion of Yq and review of the literature.
    Aiello V; Astolfi N; Gruppioni R; Buldrini B; Prontera P; Bonfatti A; Sensi A; Calzolari E
    Genet Couns; 2007; 18(4):379-82. PubMed ID: 18286818
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Inversions of chromosomes 2 and 6 in mantle cell lymphoma. Cytogenetic, FISH, and molecular studies.
    Pedrazzini E; Cerretini R; Noriega MF; Narbaitz M; Palacios MF; Negri P; Bengió R; Slavutsky I
    Cancer Genet Cytogenet; 2006 Jun; 167(2):164-7. PubMed ID: 16737918
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Deletion of 3'CBFbeta in an inv(16)(p13.lq22) ascertained by fluorescence in situ hybridization and reverse-transcriptase polymerase chain reaction.
    Hung D; St Heaps L; Benson W; Mirochnik O; Sharma P; Smith A
    Cancer Genet Cytogenet; 2007 Jan; 172(1):92-4. PubMed ID: 17175390
    [No Abstract]   [Full Text] [Related]  

  • 37. Translocation (2;11)(p21;q23) in a patient with polycythemia vera: a novel clonal chromosome abnormality.
    Acar K; Sucak GT; Yağci M; Tunca Y; Haznedar R
    Am J Hematol; 2006 Nov; 81(11):891. PubMed ID: 16804938
    [No Abstract]   [Full Text] [Related]  

  • 38. A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses.
    Mechoso B; Vaglio A; Quadrelli A; Mark HF; Huang XL; Milunsky A; Quadrelli R
    Fetal Diagn Ther; 2007; 22(4):249-53. PubMed ID: 17369689
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Chromosome segregation in an infertile man carrying a unique pericentric inversion, inv(21)(p12q22.3), analysed using fluorescence in situ hybridization on sperm nuclei: significance for clinical genetics. A case report.
    Malan V; Pipiras E; Sifer C; Kanafani S; Cedrin-Durnerin I; Martin-Pont B; Hugues JN; Wolf JP; Benzacken B
    Hum Reprod; 2006 Aug; 21(8):2052-6. PubMed ID: 16585123
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male.
    Ergul E; Liehr T; Mrasek K; Sazci A
    Fertil Steril; 2009 Jul; 92(1):391.e9-391.e12. PubMed ID: 19368909
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.