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Items: 1 to 20 of 108

1.

Prognostic Impact of del(17p) and del(22q) as assessed by interphase FISH in sporadic colorectal carcinomas.

González-González M, Muñoz-Bellvis L, Mackintosh C, Fontanillo C, Gutiérrez ML, Abad MM, Bengoechea O, Teodosio C, Fonseca E, Fuentes M, De Las Rivas J, Orfao A, Sayagués JM.

PLoS One. 2012;7(8):e42683. doi: 10.1371/journal.pone.0042683. Epub 2012 Aug 17.

2.

Intratumoural cytogenetic heterogeneity of sporadic colorectal carcinomas suggests several pathways to liver metastasis.

Sayagués JM, Abad Mdel M, Melchor HB, Gutiérrez ML, González-González M, Jensen E, Bengoechea O, Fonseca E, Orfao A, Muñoz-Bellvis L.

J Pathol. 2010 Jul;221(3):308-19. doi: 10.1002/path.2712.

PMID:
20527024
3.

Numerical abnormalities of chromosomes 17 and 18 in sporadic colorectal cancer: Incidence and correlation with clinical and biological findings and the prognosis of the disease.

Garcia J, Duran A, Tabernero MD, Garcia Plaza A, Flores Corral T, Najera ML, Gomez-Alonso A, Orfao A.

Cytometry B Clin Cytom. 2003 Jan;51(1):14-20.

4.

Chromosomal alteration in Chinese sporadic colorectal carcinomas detected by comparative genomic hybridization.

Xiao XY, Zhou XY, Yan G, Sun MH, Du X.

Diagn Mol Pathol. 2007 Jun;16(2):96-103.

PMID:
17525679
5.

Unique genetic profile of sporadic colorectal cancer liver metastasis versus primary tumors as defined by high-density single-nucleotide polymorphism arrays.

Muñoz-Bellvis L, Fontanillo C, González-González M, Garcia E, Iglesias M, Esteban C, Gutierrez ML, Abad MM, Bengoechea O, De Las Rivas J, Orfao A, Sayagués JM.

Mod Pathol. 2012 Apr;25(4):590-601. doi: 10.1038/modpathol.2011.195. Epub 2012 Jan 6.

6.

Identification of a characteristic copy number alteration profile by high-resolution single nucleotide polymorphism arrays associated with metastatic sporadic colorectal cancer.

González-González M, Fontanillo C, Abad MM, Gutiérrez ML, Mota I, Bengoechea O, Santos-Briz Á, Blanco O, Fonseca E, Ciudad J, Fuentes M, De Las Rivas J, Alcazar JA, García J, Muñoz-Bellvis L, Orfao A, Sayagués JM.

Cancer. 2014 Jul 1;120(13):1948-59. doi: 10.1002/cncr.28681. Epub 2014 Mar 25.

7.

Both chromosome 13 abnormalities by metaphase cytogenetics and deletion of 13q by interphase FISH only are prognostically relevant in multiple myeloma.

Kaufmann H, Krömer E, Nösslinger T, Weltermann A, Ackermann J, Reisner R, Bernhart M, Drach J.

Eur J Haematol. 2003 Sep;71(3):179-83.

PMID:
12930318
8.

Apparently unrelated cytogenetic abnormalities among 462 probands referred for the detection of del(22q) by FISH.

Smith A, St Heaps L, Robson L.

Am J Med Genet. 2002 Dec 15;113(4):346-50.

PMID:
12457406
9.

Recurrent deletions involving chromosomes 1, 5, 17, and 18 in colorectal carcinoma: possible role in biological and clinical behavior of tumors.

Gerdes H, Chen Q, Elahi AH, Sircar A, Goldberg E, Winawer D, Urmacher C, Winawer SJ, Jhanwar SC.

Anticancer Res. 1995 Jan-Feb;15(1):13-24.

PMID:
7733622
10.

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; AML/MDS Working Party of the Korean Society of Hematology.

Cancer Genet Cytogenet. 2010 Dec;203(2):193-202. doi: 10.1016/j.cancergencyto.2010.08.007.

PMID:
21156233
11.

Chromosome arm 20q gains and other genomic alterations in colorectal cancer metastatic to liver, as analyzed by comparative genomic hybridization and fluorescence in situ hybridization.

Korn WM, Yasutake T, Kuo WL, Warren RS, Collins C, Tomita M, Gray J, Waldman FM.

Genes Chromosomes Cancer. 1999 Jun;25(2):82-90.

PMID:
10337990
12.

Clinical and pathological significance of numerical aberrations of chromosomes 11 and 17 in colorectal neoplasms.

Tagawa Y, Yasutake T, Sawai T, Nanashima A, Jibiki M, Morinaga M, Akama F, Nakagoe T, Ayabe H.

Clin Cancer Res. 1997 Sep;3(9):1587-92.

13.

Impact of trisomy 12, del(13q), del(17p), and del(11q) on the immunophenotype, DNA ploidy status, and proliferative rate of leukemic B-cells in chronic lymphocytic leukemia.

Quijano S, López A, Rasillo A, Sayagués JM, Barrena S, Sánchez ML, Teodosio C, Giraldo P, Giralt M, Pérez MC, Romero M, Perdiguer L, Orfao A.

Cytometry B Clin Cytom. 2008 May;74(3):139-49.

14.

Progression in smoldering myeloma is independently determined by the chromosomal abnormalities del(17p), t(4;14), gain 1q, hyperdiploidy, and tumor load.

Neben K, Jauch A, Hielscher T, Hillengass J, Lehners N, Seckinger A, Granzow M, Raab MS, Ho AD, Goldschmidt H, Hose D.

J Clin Oncol. 2013 Dec 1;31(34):4325-32. doi: 10.1200/JCO.2012.48.4923. Epub 2013 Oct 21.

PMID:
24145347
15.

Mapping of genetic deletions on chromosome 3 in colorectal cancer: loss of 3p25-pter is associated with distant metastasis and poor survival.

Tsai MH, Fang WH, Lin SH, Tzeng ST, Huang CS, Yen SJ, Chou SJ, Yang YC.

Ann Surg Oncol. 2011 Sep;18(9):2662-70. doi: 10.1245/s10434-011-1603-9. Epub 2011 Feb 23.

PMID:
21347784
16.

Mapping of genetic abnormalities of primary tumours from metastatic CRC by high-resolution SNP arrays.

Sayagués JM, Fontanillo C, Abad Mdel M, González-González M, Sarasquete ME, Chillon Mdel C, Garcia E, Bengoechea O, Fonseca E, Gonzalez-Diaz M, De las Rivas J, Muñoz-Bellvis L, Orfao A.

PLoS One. 2010 Oct 29;5(10):e13752. doi: 10.1371/journal.pone.0013752.

17.

Prognostic Impact of Cytogenetic Abnormalities in Multiple Myeloma: A Retrospective Analysis of 229 Patients.

Jian Y, Chen X, Zhou H, Zhu W, Liu N, Geng C, Chen W.

Medicine (Baltimore). 2016 May;95(19):e3521. doi: 10.1097/MD.0000000000003521.

18.

Molecular cytogenetic aberrations in patients with multiple myeloma studied by interphase fluorescence in situ hybridization.

Chen L, Li J, Xu W, Qiu H, Zhu Y, Zhang Y, Duan L, Qian S, Lu H.

Exp Oncol. 2007 Jun;29(2):116-20.

PMID:
17704743
19.

Patterns of BCR/ABL gene rearrangements by interphase fluorescence in situ hybridization (FISH) in BCR/ABL+ leukemias: incidence and underlying genetic abnormalities.

Primo D, Tabernero MD, Rasillo A, Sayagués JM, Espinosa AB, Chillón MC, Garcia-Sanz R, Gutierrez N, Giralt M, Hagemeijer A, San Miguel JF, Orfao A.

Leukemia. 2003 Jun;17(6):1124-9.

PMID:
12764379
20.

Interphase cytogenetic studies of human hepatocellular carcinomas by fluorescent in situ hybridization.

Hamon-Benais C, Ingster O, Terris B, Couturier-Turpin MH, Bernheim A, Feldmann G.

Hepatology. 1996 Mar;23(3):429-35.

PMID:
8617421

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