131 related articles for article (PubMed ID: 12471217)
1. Hereditary duplication of proximal chromosome 1q (q11q22) in a patient with T lymphoblastic lymphoma/leukaemia: a family study using G banding and comparative genomic hybridisation.
Chan NP; Ng MH; Cheng SH; Lee V; Tsang KS; Lau TT; Li CK
J Med Genet; 2002 Dec; 39(12):e79. PubMed ID: 12471217
[No Abstract] [Full Text] [Related]
2. Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding. Implications for treatment stratification of childhood acute lymphoblastic leukaemia: detailed analysis of 70 cases.
Nordgren A; Heyman M; Sahlén S; Schoumans J; Söderhäll S; Nordenskjöld M; Blennow E
Eur J Haematol; 2002 Jan; 68(1):31-41. PubMed ID: 11952819
[TBL] [Abstract][Full Text] [Related]
3. Acute lymphoblastic leukemia in a patient with constitutional chromosome 1pter-p36.31 duplication and 1q43-qter deletion.
Khan S; Toews H; Wang JC; Arredondo J; Provias J; Göhring G; Barr RD
J Pediatr Hematol Oncol; 2012 Apr; 34(3):217-21. PubMed ID: 22217494
[TBL] [Abstract][Full Text] [Related]
4. A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma.
La Starza R; Crescenzi B; Pierini V; Romoli S; Gorello P; Brandimarte L; Matteucci C; Kropp MG; Barba G; Martelli MF; Mecucci C
Cancer Genet Cytogenet; 2007 May; 175(1):73-6. PubMed ID: 17498563
[TBL] [Abstract][Full Text] [Related]
5. Translocation (5;17)(q13;q21) in a case with precursor T-lymphoblastic lymphoma/leukemia.
Zamora L; Espinet B; Solé F; Salido M; Rodon N; Florensa L; Woessner S
Cancer Genet Cytogenet; 2002 Jan; 132(1):81-2. PubMed ID: 11801318
[No Abstract] [Full Text] [Related]
6. Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-banding.
Kuchinskaya E; Heyman M; Nordgren A; Schoumans J; Staaf J; Borg A; Söderhäll S; Grandér D; Nordenskjöld M; Blennow E
Br J Haematol; 2008 Mar; 140(5):572-7. PubMed ID: 18275435
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Marker chromosome 1q+ in acute lymphocytic leukemia.
Petković I; Nakić M; Tiefenbach A; Konja J; Kastelan M; Rajić L; Feminić-Kes R
Cancer Genet Cytogenet; 1987 Feb; 24(2):251-5. PubMed ID: 3466676
[TBL] [Abstract][Full Text] [Related]
9. Myeloid antigen positive acute lymphoblastic leukemia with the Philadelphia translocation and a jumping translocation of 1q in a child.
Montgomery KD; Winter SS; Frost JD; Hardekopf D; Holt K; Graham ML; Foucar K
Leukemia; 2004 Sep; 18(9):1548-50. PubMed ID: 15284862
[No Abstract] [Full Text] [Related]
10. Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia.
Calabrese G; Taraborelli T; Fantasia D; Guanciali Franchi P; Spadano A; Palka G
Haematologica; 2002 Aug; 87(8):888-9. PubMed ID: 12161369
[No Abstract] [Full Text] [Related]
11. Partial duplication of chromosome 1q preceding the development of an L3 lymphoblastic leukemia with t(8;14), secondary to treatment for Hodgkin's disease.
Zollino M; Genuardi M; De Santis R; Leone G; Marra R; Mancini R; Mango G; Neri G
Eur J Haematol; 1988 Mar; 40(3):193-7. PubMed ID: 3162717
[TBL] [Abstract][Full Text] [Related]
12. Integration of conventional cytogenetics, comparative genomic hybridisation and interphase fluorescence in situ hybridisation for the detection of genomic rearrangements in acute leukaemia.
McGrattan P; Campbell S; Cuthbert R; Jones FG; McMullin MF; Humphreys M
J Clin Pathol; 2008 Aug; 61(8):903-8. PubMed ID: 18474541
[TBL] [Abstract][Full Text] [Related]
13. De novo 1q32q44 duplication and distal 1q trisomy syndrome.
Nowaczyk MJ; Bayani J; Freeman V; Watts J; Squire J; Xu J
Am J Med Genet A; 2003 Jul; 120A(2):229-33. PubMed ID: 12833404
[TBL] [Abstract][Full Text] [Related]
14. Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping.
Nordgren A; Farnebo F; Johansson B; Holmgren G; Forestier E; Larsson C; Söderhäll S; Nordenskjöld M; Blennow E
Eur J Haematol; 2001 May; 66(5):297-304. PubMed ID: 11422408
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Molecular cytogenetic study of instability at 1q21 approximately q32 in adult acute lymphoblastic leukemia.
Specchia G; Albano F; Anelli L; Zagaria A; Liso A; Pannunzio A; Archidiacono N; Liso V; Rocchi M
Cancer Genet Cytogenet; 2005 Jan; 156(1):54-8. PubMed ID: 15588856
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 12756018
[TBL] [Abstract][Full Text] [Related]
18. Genomic instability in multiple myeloma: evidence for jumping segmental duplications of chromosome arm 1q.
Sawyer JR; Tricot G; Lukacs JL; Binz RL; Tian E; Barlogie B; Shaughnessy J
Genes Chromosomes Cancer; 2005 Jan; 42(1):95-106. PubMed ID: 15472896
[TBL] [Abstract][Full Text] [Related]
19. Characterization of chromosomal breakpoints in an ALL patient using cross-species color banding.
Koo SH; Kwon KC; Park JW; Lee YE; Kim JW
Cancer Genet Cytogenet; 2000 Jun; 119(2):118-20. PubMed ID: 10867146
[TBL] [Abstract][Full Text] [Related]
20. 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. PubMed ID: 9595040
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
