151 related articles for article (PubMed ID: 16875578)
1. [Clinical and laboratory characteristics of two acute lymphoblastic leukemia patients with dicentric (9; 20) (p11 - 13; q11)].
Gong SL; Qiu HY; Li JY; Han FL; Song XM; Huang ZX; Wang JM
Zhonghua Xue Ye Xue Za Zhi; 2006 May; 27(5):306-9. PubMed ID: 16875578
[TBL] [Abstract][Full Text] [Related]
2. A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11).
Slater R; Smit E; Kroes W; Bellomo MJ; Mühlematter D; Harbott J; Behrendt H; Hählen K; Veerman AJ; Hagemeijer A
Leukemia; 1995 Oct; 9(10):1613-9. PubMed ID: 7564498
[TBL] [Abstract][Full Text] [Related]
3. Cytogenetic study of a patient with infant acute lymphoblastic leukemia using GTG-banding and chromosome painting.
Alter D; Mark HF
Exp Mol Pathol; 2000 Oct; 69(2):152-8. PubMed ID: 11001863
[TBL] [Abstract][Full Text] [Related]
4. Complex chromosome 9, 20, and 22 rearrangements in acute lymphoblastic leukemia with duplication of BCR and ABL sequences.
Stevens-Kroef MJ; Dirckx R; Meers LE; Albrechts JC; Schouten HC; Hamers AJ
Cancer Genet Cytogenet; 2000 Jan; 116(2):119-23. PubMed ID: 10640143
[TBL] [Abstract][Full Text] [Related]
5. dic(9;20): a new recurrent chromosome abnormality in adult acute lymphoblastic leukemia.
Rieder H; Schnittger S; Bodenstein H; Schwonzen M; Wörmann B; Berkovic D; Ludwig WD; Hoelzer D; Fonatsch C
Genes Chromosomes Cancer; 1995 May; 13(1):54-61. PubMed ID: 7541644
[TBL] [Abstract][Full Text] [Related]
6. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
Tharapel AT; Qumsiyeh MB; Martens PR; Tharapel SA; Dalton JD; Ward JC; Wilroy RS
Am J Med Genet; 1991 Jul; 40(1):117-20. PubMed ID: 1887840
[TBL] [Abstract][Full Text] [Related]
7. Dicentric (9;20)(p11;q11) identified by fluorescence in situ hybridization in four pediatric acute lymphoblastic leukemia patients.
Heerema NA; Maben KD; Bernstein J; Breitfeld PP; Neiman RS; Vance GH
Cancer Genet Cytogenet; 1996 Dec; 92(2):111-5. PubMed ID: 8976366
[TBL] [Abstract][Full Text] [Related]
8. [Chromosome t (4; 11) acute lymphoblastic leukemia: an analysis of 10 cases].
Guo Y; Xue Y; Xie X; Lu D; Geng M
Zhonghua Xue Ye Xue Za Zhi; 2000 Feb; 21(2):71-3. PubMed ID: 11876961
[TBL] [Abstract][Full Text] [Related]
9. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.
Wang JC; Nemana L; Kou SY; Habibian R; Hajianpour MJ
Am J Med Genet; 1997 Sep; 71(4):463-6. PubMed ID: 9286456
[TBL] [Abstract][Full Text] [Related]
10. [Detection of aberrant chromosomes in acute lymphoblastic leukemia by fluorescence in situ hybridization].
Yang K; Huang L
Zhonghua Xue Ye Xue Za Zhi; 1999 Dec; 20(12):640-2. PubMed ID: 11721367
[TBL] [Abstract][Full Text] [Related]
11. Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridization.
Zhao J; Gordon PL; Wilroy RS; Martens PR; Tarleton J; Shulman LP; Simpson JL; Elias S; Tharapel AT
Am J Med Genet; 1995 May; 56(4):398-402. PubMed ID: 7604849
[TBL] [Abstract][Full Text] [Related]
12. Monosomy 20 as a pointer to dicentric (9;20) in acute lymphoblastic leukemia.
Clark R; Byatt SA; Bennett CF; Brama M; Martineau M; Moorman AV; Roberts K; Secker-Walker LM; Richards S; Eden OB; Goldstone AH; Harrison CJ
Leukemia; 2000 Feb; 14(2):241-6. PubMed ID: 10673740
[TBL] [Abstract][Full Text] [Related]
13. Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis.
Elghezal H; Le Guyader G; Radford-Weiss I; Perot C; Van Den Akker J; Eydoux P; Vekemans M; Romana SP
Genes Chromosomes Cancer; 2001 Apr; 30(4):383-92. PubMed ID: 11241791
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. The t(14;18) in a patient with de novo acute lymphoblastic leukemia is associated with t(8;9).
Lillington DM; Monard S; Johnson PW; Evans ML; Kearney LU; Lister TA; Young BD; Gibbons B
Leukemia; 1994 Apr; 8(4):560-3. PubMed ID: 8152251
[TBL] [Abstract][Full Text] [Related]
16. FISH analysis of translocations involving the short arm of chromosome 9 in lymphoid malignancies.
Leblanc T; Derré J; Flexor M; Le Coniat M; Leroux D; Rimokh R; Larsen CJ; Berger R
Genes Chromosomes Cancer; 1997 Aug; 19(4):273-7. PubMed ID: 9258663
[TBL] [Abstract][Full Text] [Related]
17. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
Wang JC; Mamunes P; Kou SY; Schmidt J; Mao R; Hsu WT
Am J Med Genet; 1998 Dec; 80(4):418-22. PubMed ID: 9856575
[TBL] [Abstract][Full Text] [Related]
18. A new complex variant Philadelphia chromosome, t(1;9;22)ins(17;22), characterized by fluorescence in situ hybridization in an adult ALL.
Fan YS; Rizkalla K; Barr RM
Leuk Res; 1999 Nov; 23(11):1001-6. PubMed ID: 10576504
[TBL] [Abstract][Full Text] [Related]
19. [Characterization of chromosomal rearrangements by in situ hybridization in glioblastoma].
Bourgeois CA; Kokalj-Vokac N; Dutrillaux AM; Poisson M; Delattre JY; Vega F; Malfoy B; Dutrillaux B
Bull Cancer; 1994 May; 81(5):360-5. PubMed ID: 7538360
[TBL] [Abstract][Full Text] [Related]
20. New recurring chromosomal translocations in childhood acute lymphoblastic leukemia.
Raimondi SC; Privitera E; Williams DL; Look AT; Behm F; Rivera GK; Crist WM; Pui CH
Blood; 1991 May; 77(9):2016-22. PubMed ID: 2018838
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
