326 related articles for article (PubMed ID: 19100515)
1. Inverted duplication dup(1)(q32q21) as sole aberration in lymphoid and myeloid malignancies.
Bacher U; Schnittger S; Grüneisen A; Haferlach T; Kern W; Haferlach C
Cancer Genet Cytogenet; 2009 Jan; 188(2):108-11. PubMed ID: 19100515
[TBL] [Abstract][Full Text] [Related]
2. Pattern of trisomy 1q in hematological malignancies: a single institution experience.
Djordjević V; Dencić-Fekete M; Jovanović J; Drakulić D; Stevanović M; Janković G; Gotić M
Cancer Genet Cytogenet; 2008 Oct; 186(1):12-8. PubMed ID: 18786437
[TBL] [Abstract][Full Text] [Related]
3. dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes.
Alfaro R; Pérez-Granero A; Durán MA; Besalduch J; Rosell J; Bernués M
Leuk Res; 2008 Jan; 32(1):159-61. PubMed ID: 17509681
[TBL] [Abstract][Full Text] [Related]
4. Partial tandem duplication of ALL1 as a recurrent molecular defect in acute myeloid leukemia with trisomy 11.
Caligiuri MA; Strout MP; Schichman SA; Mrózek K; Arthur DC; Herzig GP; Baer MR; Schiffer CA; Heinonen K; Knuutila S; Nousiainen T; Ruutu T; Block AW; Schulman P; Pedersen-Bjergaard J; Croce CM; Bloomfield CD
Cancer Res; 1996 Mar; 56(6):1418-25. PubMed ID: 8640834
[TBL] [Abstract][Full Text] [Related]
5. FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12.
Dierlamm J; Wlodarska I; Michaux L; Vermeesch JR; Meeus P; Stul M; Criel A; Verhoef G; Thomas J; Delannoy A; Louwagie A; Cassiman JJ; Mecucci C; Hagemeijer A; Van den Berghe H
Genes Chromosomes Cancer; 1997 Oct; 20(2):155-66. PubMed ID: 9331566
[TBL] [Abstract][Full Text] [Related]
6. Prognostic significance of del(20q) in patients with hematological malignancies.
Brezinová J; Zemanová Z; Ransdorfová S; Sindelárová L; Sisková M; Neuwirtová R; Cermák J; Michalová K
Cancer Genet Cytogenet; 2005 Jul; 160(2):188-92. PubMed ID: 15993278
[TBL] [Abstract][Full Text] [Related]
7. Deletion (11)(q13) as the sole anomaly in myeloid malignancies: four new cases and a short review.
Panani AD; Pappa V; Papageorgiou S; Stamatelli F; Raptis SA
Ann Hematol; 2004 Mar; 83(3):153-5. PubMed ID: 15064863
[TBL] [Abstract][Full Text] [Related]
8. Inversion of chromosome 11 inv(11)(p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: identification of a P1 clone spanning the 11q22 breakpoint.
Kobayashi H; Arai Y; Hosoda F; Maseki N; Hayashi Y; Eguchi H; Ohki M; Kaneko Y
Genes Chromosomes Cancer; 1997 Jul; 19(3):150-5. PubMed ID: 9218995
[TBL] [Abstract][Full Text] [Related]
9. Duplication of chromosome 1 [dup(1)(q21q32)] as the sole cytogenetic abnormality in a patient previously treated for AML.
Beach DF; Barnoski BL; Aviv H; Patel V; Schwarting R; Strair R; Lachant NA
Cancer Genet; 2012 Dec; 205(12):665-8. PubMed ID: 23168243
[TBL] [Abstract][Full Text] [Related]
10. [Clinical and experimental study of 38 cases with trisomy 8].
Xu WL; Jin J; Chen ZM; Lou JY; Yu YB
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec; 20(6):528-31. PubMed ID: 14669224
[TBL] [Abstract][Full Text] [Related]
11. Chromosome 1 abnormalities in myeloid malignancies: a literature survey and karyotype-phenotype associations.
Caramazza D; Hussein K; Siragusa S; Pardanani A; Knudson RA; Ketterling RP; Tefferi A
Eur J Haematol; 2010 Mar; 84(3):191-200. PubMed ID: 20002154
[TBL] [Abstract][Full Text] [Related]
12. [Abnormalities of chromosome 17 in myeloid malignancies with complex chromosomal abnormalities].
Zhu Y; Xu W; Liu Q; Pan J; Qiu H; Wang R; Qiao C; Jiang Y; Zhang S; Fan L; Zhang J; Shen Y; Xue Y; Li J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):579-82. PubMed ID: 18841577
[TBL] [Abstract][Full Text] [Related]
13. Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies.
Brezinová J; Zemanová Z; Ransdorfová S; Pavlistová L; Babická L; Housková L; Melichercíková J; Sisková M; Cermák J; Michalová K
Cancer Genet Cytogenet; 2007 Feb; 173(1):10-6. PubMed ID: 17284364
[TBL] [Abstract][Full Text] [Related]
14. Duplications of the long arm of both chromosome 1, dup(1)(q21q32), leading to tetrasomy 1q in myelodysplastic syndrome.
Kim JE; Woo KS; Kim KE; Kim SH; Park JI; Shaffer LG; Han JY
Leuk Res; 2010 Aug; 34(8):e210-2. PubMed ID: 20299094
[No Abstract] [Full Text] [Related]
15. 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]
16. Role of chromosome 1 pericentric heterochromatin (1q) in pathogenesis of myelodysplastic syndromes: report of 2 new cases.
Millington K; Hudnall SD; Northup J; Panova N; Velagaleti G
Exp Mol Pathol; 2008 Apr; 84(2):189-93. PubMed ID: 18339374
[TBL] [Abstract][Full Text] [Related]
17. Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpoints.
Heller A; Loncarevic IF; Glaser M; Gebhart E; Trautmann U; Claussen U; Liehr T
Int J Oncol; 2004 Jan; 24(1):127-36. PubMed ID: 14654949
[TBL] [Abstract][Full Text] [Related]
18. Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases.
Beyer V; Mühlematter D; Parlier V; Cabrol C; Bougeon-Mamin S; Solenthaler M; Tobler A; Pugin P; Gregor M; Hitz F; Hess U; Chapuis B; Laurencet F; Schanz U; Schmidt PM; van Melle G; Jotterand M
Cancer Genet Cytogenet; 2005 Jul; 160(2):97-119. PubMed ID: 15993266
[TBL] [Abstract][Full Text] [Related]
19. Derivative (1)t(1;16)(p11;p11.1) in myelodysplastic syndrome: a case report and review of the literature.
Lunghi M; Casorzo L; De Paoli L; Riccomagno P; Rossi D; Gaidano G
Cancer Genet Cytogenet; 2010 Jan; 196(1):89-92. PubMed ID: 19963141
[TBL] [Abstract][Full Text] [Related]
20. Derivative (1;18)(q10;q10): a recurrent and novel unbalanced translocation involving 1q in myeloid disorders.
Wan TS; Ma SK; Au WY; Chan LC
Cancer Genet Cytogenet; 2001 Jul; 128(1):35-8. PubMed ID: 11454427
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
