230 related articles for article (PubMed ID: 26136832)
1. High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia.
Othman MA; Melo JB; Carreira IM; Rincic M; Glaser A; Grygalewicz B; Gruhn B; Wilhelm K; Rittscher K; Meyer B; Silva ML; de Jesus Marques Salles T; Liehr T
Mol Cytogenet; 2015; 8():45. PubMed ID: 26136832
[TBL] [Abstract][Full Text] [Related]
2. Comprehensive chronic lymphocytic leukemia diagnostics by combined multiplex ligation dependent probe amplification (MLPA) and interphase fluorescence in situ hybridization (iFISH).
Alhourani E; Rincic M; Othman MA; Pohle B; Schlie C; Glaser A; Liehr T
Mol Cytogenet; 2014; 7(1):79. PubMed ID: 25435911
[TBL] [Abstract][Full Text] [Related]
3. Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches.
Karst C; Gross M; Haase D; Wedding U; Höffken K; Liehr T; Mkrtchyan H
Int J Oncol; 2006 Apr; 28(4):891-7. PubMed ID: 16525638
[TBL] [Abstract][Full Text] [Related]
4. A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia.
Othman MA; Rincic M; Melo JB; Carreira IM; Alhourani E; Hunstig F; Glaser A; Liehr T
Leuk Res Treatment; 2014; 2014():357123. PubMed ID: 25374696
[TBL] [Abstract][Full Text] [Related]
5. Routine application of a novel MLPA-based first-line screening test uncovers clinically relevant copy number aberrations in haematological malignancies undetectable by conventional cytogenetics.
Konialis C; Savola S; Karapanou S; Markaki A; Karabela M; Polychronopoulou S; Ampatzidou M; Voulgarelis M; Viniou NA; Variami E; Koumarianou A; Zoi K; Hagnefelt B; Schouten JP; Pangalos C
Hematology; 2014 Jun; 19(4):217-24. PubMed ID: 23928116
[TBL] [Abstract][Full Text] [Related]
6. Evaluation of multiplex ligation dependent probe amplification (MLPA) for identification of acute lymphoblastic leukemia with an intrachromosomal amplification of chromosome 21 (iAMP21) in a Brazilian population.
Fuka G; Farias-Vieira TM; Hummel L; Blunck CB; Santoro JC; Terra-Granado E; Barbosa TC; Emerenciano M; Pombo-de-Oliveira MS
Mol Cytogenet; 2015; 8():35. PubMed ID: 26060508
[TBL] [Abstract][Full Text] [Related]
7. Three novel cytogenetically cryptic EVI1 rearrangements associated with increased EVI1 expression and poor prognosis identified in 27 acute myeloid leukemia cases.
Haferlach C; Bacher U; Grossmann V; Schindela S; Zenger M; Kohlmann A; Kern W; Haferlach T; Schnittger S
Genes Chromosomes Cancer; 2012 Dec; 51(12):1079-85. PubMed ID: 22887804
[TBL] [Abstract][Full Text] [Related]
8. Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization are complementary techniques to detect cytogenetic abnormalities in multiple myeloma.
Alpar D; de Jong D; Holczer-Nagy Z; Kajtar B; Savola S; Jakso P; David M; Kosztolanyi S; Kereskai L; Pajor L; Szuhai K
Genes Chromosomes Cancer; 2013 Sep; 52(9):785-93. PubMed ID: 23720363
[TBL] [Abstract][Full Text] [Related]
9. Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes.
Slovak ML; Smith DD; Bedell V; Hsu YH; O'Donnell M; Forman SJ; Gaal K; McDaniel L; Schultz R; Ballif BC; Shaffer LG
Mol Cytogenet; 2010 Nov; 3():23. PubMed ID: 21078186
[TBL] [Abstract][Full Text] [Related]
10. [Cytogenetic and FISH findings are complementary in childhood ALL].
Haltrich I; Csóka M; Kovács G; Fekete G
Magy Onkol; 2008 Sep; 52(3):283-91. PubMed ID: 18845499
[TBL] [Abstract][Full Text] [Related]
11. Rapid Identification of Key Copy Number Alterations in B- and T-Cell Acute Lymphoblastic Leukemia by Digital Multiplex Ligation-Dependent Probe Amplification.
Thakral D; Kaur G; Gupta R; Benard-Slagter A; Savola S; Kumar I; Anand R; Rani L; Verma P; Joshi S; Kumar L; Sharma A; Bakhshi S; Seth R; Singh V
Front Oncol; 2019; 9():871. PubMed ID: 31572674
[TBL] [Abstract][Full Text] [Related]
12. Novel Cryptic Rearrangements in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Involving the MLL Gene.
Othman MA; Grygalewicz B; Pienkowska-Grela B; Rincic M; Rittscher K; Melo JB; Carreira IM; Meyer B; Marzena W; Liehr T
J Histochem Cytochem; 2015 May; 63(5):384-90. PubMed ID: 25699572
[TBL] [Abstract][Full Text] [Related]
13. Oligo-based aCGH analysis reveals cryptic unbalanced der(6)t(X;6) in pediatric t(12;21)-positive acute lymphoblastic leukemia.
Kjeldsen E
Exp Mol Pathol; 2016 Aug; 101(1):38-43. PubMed ID: 27215399
[TBL] [Abstract][Full Text] [Related]
14. Chromosomal microarray analysis is superior in identifying cryptic aberrations in patients with acute lymphoblastic leukemia at diagnosis/relapse as a single assay.
Chen C; Heng EYH; Lim AST; Lau LC; Lim TH; Wong GC; Tien SL
Int J Lab Hematol; 2019 Aug; 41(4):561-571. PubMed ID: 31112375
[TBL] [Abstract][Full Text] [Related]
15. Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias.
Andreasson P; Höglund M; Békássy AN; Garwicz S; Heldrup J; Mitelman F; Johansson B
Eur J Haematol; 2000 Jul; 65(1):40-51. PubMed ID: 10914938
[TBL] [Abstract][Full Text] [Related]
16. Hidden aberrations diagnosed by interphase fluorescence in situ hybridisation and spectral karyotyping in childhood acute lymphoblastic leukaemia.
Nordgren A
Leuk Lymphoma; 2003 Dec; 44(12):2039-53. PubMed ID: 14959846
[TBL] [Abstract][Full Text] [Related]
17. Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH.
Van Limbergen H; Poppe B; Michaux L; Herens C; Brown J; Noens L; Berneman Z; De Bock R; De Paepe A; Speleman F
Genes Chromosomes Cancer; 2002 Jan; 33(1):60-72. PubMed ID: 11746988
[TBL] [Abstract][Full Text] [Related]
18. MLLT10 and IL3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia: A case report.
Othman MA; Melo JB; Carreira IM; Rincic M; Alhourani E; Wilhelm K; Gruhn B; Glaser A; Liehr T
Oncol Rep; 2015 Feb; 33(2):625-30. PubMed ID: 25435396
[TBL] [Abstract][Full Text] [Related]
19. Close correlation of copy number aberrations detected by next-generation sequencing with results from routine cytogenetics in acute myeloid leukemia.
Vosberg S; Herold T; Hartmann L; Neumann M; Opatz S; Metzeler KH; Schneider S; Graf A; Krebs S; Blum H; Baldus CD; Hiddemann W; Spiekermann K; Bohlander SK; Mansmann U; Greif PA
Genes Chromosomes Cancer; 2016 Jul; 55(7):553-67. PubMed ID: 27015608
[TBL] [Abstract][Full Text] [Related]
20. Integration of microarray analysis into the clinical diagnosis of hematological malignancies: How much can we improve cytogenetic testing?
Peterson JF; Aggarwal N; Smith CA; Gollin SM; Surti U; Rajkovic A; Swerdlow SH; Yatsenko SA
Oncotarget; 2015 Aug; 6(22):18845-62. PubMed ID: 26299921
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
