These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 2073840)

  • 21. [The chromosome 13 in ring syndrome].
    Giraud F; Emberger JM; Pinsard N; Mattei JF; Mattei MG
    Pediatrie; 1975 Jun; 30(4):339-49. PubMed ID: 1178264
    [No Abstract]   [Full Text] [Related]  

  • 22. Report of the committee on chromosome changes in neoplasia.
    Mitelman F; Kaneko Y; Trent JM
    Cytogenet Cell Genet; 1990; 55(1-4):358-86. PubMed ID: 2073841
    [No Abstract]   [Full Text] [Related]  

  • 23. DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.
    Demczuk S; Aurias A
    Ann Genet; 1995; 38(2):59-76. PubMed ID: 7486827
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
    Koiffmann CP; Gonzalez CH; Vianna-Morgante AM; Kim CA; Odone-Filho V; Wajntal A
    Am J Med Genet; 1995 Jul; 58(1):46-9. PubMed ID: 7573155
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cytogenetic features of 5q deletion and 5q- syndrome in myelodysplastic syndrome in Korea; marker chromosomes proved to be chromosome 5 with interstitial deletion by fluorescence in situ hybridization.
    Lee HR; Oh B; Hong DS; Zang DY; Yoon HJ; Kim HJ; Kim I; Ahn JS; Cheong JW; Lee KA; Cho KS; Lee MH; Bang SM; Kim TY; Yun YM; Min YH; Lee YK; Lee DS;
    Cancer Genet Cytogenet; 2010 Dec; 203(2):193-202. PubMed ID: 21156233
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Neuroblastoma in patients with constitutional chromosomal changes.
    Fryns JP
    Genet Couns; 1996; 7(1):73. PubMed ID: 8652093
    [No Abstract]   [Full Text] [Related]  

  • 27. The chromosome, its anatomy, and its aberrations.
    Yang-Feng TL
    Res Publ Assoc Res Nerv Ment Dis; 1991; 69():19-38. PubMed ID: 2003160
    [No Abstract]   [Full Text] [Related]  

  • 28. [Chromosome abnormalities in early cancers].
    Maeda S; Horio M; Kitazawa S; Sugiyama T
    Gan No Rinsho; 1988 Aug; 34(10):1264-72. PubMed ID: 3172486
    [TBL] [Abstract][Full Text] [Related]  

  • 29. In situ hybridization of fluorescent probes on chromosomes, nuclei or stretched DNA: applications in physical mapping and characterization of genomic rearrangements.
    Desmaze C; Aurias A
    Cell Mol Biol (Noisy-le-grand); 1995 Nov; 41(7):925-31. PubMed ID: 8595371
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genes and chromosomes in human cancer.
    Yunis JJ
    Prog Med Virol; 1985; 32():58-71. PubMed ID: 3895299
    [No Abstract]   [Full Text] [Related]  

  • 31. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F; Ledbetter DH
    Am J Med Genet; 1987 Dec; 28(4):813-20. PubMed ID: 3688019
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Chromosomal changes in primary myelodysplasias].
    Iavorkovskiĭ LI; Riauzova LIu; Soloveĭ EIa; Iavorkovskiĭ LL
    Eksp Onkol; 1990; 12(2):10-6. PubMed ID: 2180674
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Human embryonic stem cells as models for aneuploid chromosomal syndromes.
    Biancotti JC; Narwani K; Buehler N; Mandefro B; Golan-Lev T; Yanuka O; Clark A; Hill D; Benvenisty N; Lavon N
    Stem Cells; 2010 Sep; 28(9):1530-40. PubMed ID: 20641042
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chromosomes as markers in human cancer.
    Sandberg AA
    Int Adv Surg Oncol; 1981; 4():311-36. PubMed ID: 7019095
    [No Abstract]   [Full Text] [Related]  

  • 35. Cytogenetic analysis in patients with myelodysplastic syndrome.
    Hu N; Bian M
    Proc Chin Acad Med Sci Peking Union Med Coll; 1990; 5(3):135-9. PubMed ID: 2098765
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Chromosomal abnormalities in hematologic malignant diseases.
    Le Beau MM
    Prog Clin Biol Res; 1990; 340B():325-35. PubMed ID: 2203012
    [No Abstract]   [Full Text] [Related]  

  • 37. [Mental retardation and sexual development in chromosomal syndrome (author's transl)].
    Balestrazzi P; Bernasconi S; Medioli FC; Corrini L; Villani G
    Ateneo Parmense Acta Biomed; 1980; 51(1):45-51. PubMed ID: 7470180
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Characterisation of supernumerary chromosomal markers: a study of 13 cases.
    Douet-Guilbert N; Marical H; Pinson L; Herry A; Le Bris MJ; Morel F; De Braekeleer M
    Cytogenet Genome Res; 2007; 116(1-2):18-23. PubMed ID: 17268173
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Chromosomal syndromes.
    Shiang R
    Atlas Oral Maxillofac Surg Clin North Am; 2014 Sep; 22(2):197-203. PubMed ID: 25172000
    [No Abstract]   [Full Text] [Related]  

  • 40. Complex chromosomal rearrangement involving chromosomes 11, 13 and 21.
    Kleczkowska A; Fryns JP; Jaeken J; Van den Berghe H
    Ann Genet; 1988; 31(2):126-8. PubMed ID: 3261149
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.