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Items: 1 to 20 of 87

1.

Fast approach for clarification of chromosomal aberrations by using LM-PCR and FT-CGH in leukaemic sample.

Dittmann K, Przybylski GK, Grabarczyk P, Dölken G, Gesk S, Siebert R, Schmidt CA.

Acta Haematol. 2012;127(1):16-9. doi: 10.1159/000330519. Epub 2011 Oct 7.

2.

Molecular characterization of a novel chromosomal translocation t(12;14)(q23;q11.2) in T-lymphoblastic lymphoma between the T-cell receptor delta-deleting elements (TRDREC and TRAJ61) and the hypothetical gene C12orf42.

Przybylski GK, Dittmann K, Grabarczyk P, Dölken G, Gesk S, Harder L, Landmann E, Siebert R, Schmidt CA.

Eur J Haematol. 2010 Nov;85(5):452-6. doi: 10.1111/j.1600-0609.2010.01508.x.

PMID:
20659153
3.

Efficacy of high-resolution comparative genomic hybridization (HR-CGH) in detection of chromosomal abnormalities in children with acute leukaemia.

Vranova V, Mentzlova D, Oltova A, Linkova V, Zezulkova D, Filkova H, Mendelova D, Sterba J, Kuglik P.

Neoplasma. 2008;55(1):23-30.

PMID:
18190236
4.

Comparative genomic hybridization is a powerful tool, complementary to cytogenetics, to identify chromosomal abnormalities in childhood acute lymphoblastic leukaemia.

Paszek-Vigier M, Talmant P, Méchinaud F, Garand R, Harousseau JL, Bataille R, Avet-Loiseau H.

Br J Haematol. 1997 Dec;99(3):589-96.

PMID:
9401071
5.

Phenotypic and genetic characterization of adult T-cell acute lymphoblastic leukemia with del(9)(q34);SET-NUP214 rearrangement.

Chae H, Lim J, Kim M, Park J, Kim Y, Han K, Lee S, Min WS.

Ann Hematol. 2012 Feb;91(2):193-201. doi: 10.1007/s00277-011-1289-x. Epub 2011 Jul 1.

PMID:
21720744
6.

Comparative genomic hybridization-aided unraveling of complex karyotypes in human hematopoietic neoplasias.

Verdorfer I, Brecevic L, Saul W, Schenker B, Kirsch M, Trautmann U, Helm G, Gramatzki M, Gebhart E.

Cancer Genet Cytogenet. 2001 Jan 1;124(1):1-6.

PMID:
11165314
7.

Structural and numerical abnormalities resolved in one-step analysis: the most common chromosomal rearrangements detected by comparative genomic hybridization in childhood acute lymphoblastic leukemia.

Kowalczyk JR, Babicz M, Gaworczyk A, Lejman M, Winnicka D, Styka B, Jaszczuk I.

Cancer Genet Cytogenet. 2010 Jul 15;200(2):161-6. doi: 10.1016/j.cancergencyto.2010.04.016.

PMID:
20620600
8.

Importance of using comparative genomic hybridization to improve detection of chromosomal changes in childhood acute lymphoblastic leukemia.

Jarosová M, Holzerová M, Jedlicková K, Mihál V, Zuna J, Starý J, Pospísilová D, Zemanová Z, Trka J, Blazek J, Pikalová Z, Indrák K.

Cancer Genet Cytogenet. 2000 Dec;123(2):114-22.

PMID:
11156736
9.

Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors.

Kallioniemi OP, Kallioniemi A, Piper J, Isola J, Waldman FM, Gray JW, Pinkel D.

Genes Chromosomes Cancer. 1994 Aug;10(4):231-43. Review.

PMID:
7522536
10.

A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia.

Soulier J, Pierron G, Vecchione D, Garand R, Brizard F, Sigaux F, Stern MH, Aurias A.

Genes Chromosomes Cancer. 2001 Jul;31(3):248-54.

PMID:
11391795
11.

Nonrandom chromosomal imbalances in primary mediastinal B-cell lymphoma detected by arbitrarily primed PCR fingerprinting.

Scarpa A, Taruscio D, Scardoni M, Iosi F, Paradisi S, Ennas MG, Rigaud G, Moore PS, Menestrina F.

Genes Chromosomes Cancer. 1999 Nov;26(3):203-9.

PMID:
10502317
12.

Complex and cryptic chromosomal rearrangements involving the MLL gene in acute leukemia: a study of 7 patients and review of the literature.

De Braekeleer E, Meyer C, Douet-Guilbert N, Morel F, Le Bris MJ, Berthou C, Arnaud B, Marschalek R, Férec C, De Braekeleer M.

Blood Cells Mol Dis. 2010 Apr 15;44(4):268-74. doi: 10.1016/j.bcmd.2010.02.011. Epub 2010 Mar 4. Review.

PMID:
20206559
13.

High-resolution comparative genomic hybridisation yields a high detection rate of chromosomal aberrations in childhood acute lymphoblastic leukaemia.

Kristensen TD, Wesenberg F, Jonsson OG, Carlsen NT, Forestier E, Kirchhoff M, Lundsteen C, Schmiegelow K.

Eur J Haematol. 2003 Jun;70(6):363-72.

PMID:
12756018
14.

High incidence of unbalanced chromosomal changes in mantle cell lymphoma detected by comparative genomic hybridization.

Jarosová M, Papajík T, Holzerová M, Dusek L, Pikalová Z, Lakomá I, Raida L, Faber E, Divoká M, Vlachová S, Prekopová I, Novosadová A, Pospísilová H, Indrák K.

Leuk Lymphoma. 2004 Sep;45(9):1835-46.

PMID:
15223644
15.

Chromosomal aberrations in follicular non-Hodgkin lymphomas of Japanese patients, detected with comparative genomic hybridization and polymerase chain reaction analysis.

D'Haese JG, Tsukasaki K, Cremer FW, Fischer C, Bartram CR, Jauch A.

Cancer Genet Cytogenet. 2005 Oct 15;162(2):107-14.

PMID:
16213357
16.

Value of comparative genomic hybridization and fluorescence in situ hybridization for molecular diagnostics in multiple myeloma.

Liebisch P, Viardot A, Bassermann N, Wendl C, Roth K, Goldschmidt H, Einsele H, Straka C, Stilgenbauer S, Döhner H, Bentz M.

Br J Haematol. 2003 Jul;122(2):193-201.

PMID:
12846886
17.

Chromosomal imbalances in diffuse large B-cell lymphoma detected by comparative genomic hybridization.

Berglund M, Enblad G, Flordal E, Lui WO, Backlin C, Thunberg U, Sundström C, Roos G, Allander SV, Erlanson M, Rosenquist R, Larsson C, Lagercrantz S.

Mod Pathol. 2002 Aug;15(8):807-16.

18.

Detection of chromosome over- and underrepresentations in hyperdiploid acute lymphoblastic leukemia by comparative genomic hybridization.

Wong N, Chen SJ, Cao Q, Su XY, Niu C, Wu QW, Leung TW, Wickham N, Johnson PJ, Chen Z.

Cancer Genet Cytogenet. 1998 May;103(1):20-4.

PMID:
9595040
20.

Genetic aberrations in pediatric acute lymphoblastic leukemia by comparative genomic hybridization.

Karhu R, Siitonen S, Tanner M, Keinänen M, Mäkipernaa A, Lehtinen M, Vilpo JA, Isola J.

Cancer Genet Cytogenet. 1997 Jun;95(2):123-9.

PMID:
9169028

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