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.
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]
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]
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]