125 related articles for article (PubMed ID: 12472589)
21. A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies.
MacKinnon RN; Campbell LJ
Cancer Genet Cytogenet; 2005 Dec; 163(2):176-9. PubMed ID: 16337864
[TBL] [Abstract][Full Text] [Related]
22. Cytogenetic abnormalities in myelodysplastic syndrome: an overview.
Kawankar N; Vundinti BR
Hematology; 2011 May; 16(3):131-8. PubMed ID: 21669051
[TBL] [Abstract][Full Text] [Related]
23. Isochromosome 7q in Down syndrome.
Wong KF; Lam SC; Leung JN
Cancer Genet Cytogenet; 2006 Jan; 164(2):152-4. PubMed ID: 16434320
[TBL] [Abstract][Full Text] [Related]
24. Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.
Valli R; De Paoli E; Nacci L; Frattini A; Pasquali F; Maserati E
Pediatr Blood Cancer; 2017 Aug; 64(8):. PubMed ID: 28130858
[TBL] [Abstract][Full Text] [Related]
25. Isochromosome 7q and Wilms tumor.
Sandoval C; Stringel G; Ozkaynak MF; Tugal O; Jayabose S
Cancer Genet Cytogenet; 1998 Jul; 104(1):61-5. PubMed ID: 9648561
[TBL] [Abstract][Full Text] [Related]
26. Isochromosome 17q in MDS: a marker of a distinct entity.
Pinheiro RF; Chauffaille Mde L; Silva MR
Cancer Genet Cytogenet; 2006 Apr; 166(2):189-90. PubMed ID: 16631479
[No Abstract] [Full Text] [Related]
27. Myelodysplastic syndrome associated with monosomy 7 in childhood: a retrospective study.
Aktas D; Tuncbilek E
Cancer Genet Cytogenet; 2006 Nov; 171(1):72-5. PubMed ID: 17074595
[TBL] [Abstract][Full Text] [Related]
28. Mutation analysis of SBDS in pediatric acute myeloblastic leukemia.
Majeed F; Jadko S; Freedman MH; Dror Y
Pediatr Blood Cancer; 2005 Dec; 45(7):920-4. PubMed ID: 16007594
[TBL] [Abstract][Full Text] [Related]
29. Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course.
McClure RF; Dewald GW; Hoyer JD; Hanson CA
Br J Haematol; 1999 Aug; 106(2):445-54. PubMed ID: 10460605
[TBL] [Abstract][Full Text] [Related]
30. Pentasomy 8q in myelodysplasia.
Kwong YL; Chan TK
Cancer Genet Cytogenet; 1998 Jan; 100(2):179-81. PubMed ID: 9428366
[TBL] [Abstract][Full Text] [Related]
31. Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH).
Tosi S; Harbott J; Haas OA; Douglas A; Hughes DM; Ross FM; Biondi A; Scherer SW; Kearney L
Leukemia; 1996 Apr; 10(4):644-9. PubMed ID: 8618441
[TBL] [Abstract][Full Text] [Related]
32. Isochromosomes in acute lymphoblastic leukaemia: i(21q) is a significant finding.
Martineau M; Clark R; Farrell DM; Hawkins JM; Moorman AV; Secker-Walker LM
Genes Chromosomes Cancer; 1996 Sep; 17(1):21-30. PubMed ID: 8889503
[TBL] [Abstract][Full Text] [Related]
33. An isochromosome of the long arm of chromosome 18 in a patient with myelodysplastic syndrome with myelofibrosis.
Xue Y; Cao Y; Gao Y; Xie X; Lu D; Chen Z
Cancer Genet Cytogenet; 1995 Feb; 79(2):149-52. PubMed ID: 7889509
[TBL] [Abstract][Full Text] [Related]
34. Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype.
Cuneo A; Bigoni R; Cavazzini F; Bardi A; Roberti MG; Agostini P; Tammiso E; Ciccone N; Mancini M; Nanni M; De Cuia R; Divona M; La Starza R; Crescenzi B; Testoni N; Rege Cambrin G; Mecucci C; Lo Coco F; Saglio G; Castoldi G
Leukemia; 2002 Sep; 16(9):1745-51. PubMed ID: 12200689
[TBL] [Abstract][Full Text] [Related]
35. Maternal isochromosome 7q and paternal isochromosome 7p in a boy with growth retardation.
Kotzot D; Holland H; Keller E; Froster UG
Am J Med Genet; 2001 Aug; 102(2):169-72. PubMed ID: 11477611
[TBL] [Abstract][Full Text] [Related]
36. Conventional and molecular cytogenetic features of myelodysplastic syndrome in China.
Chen L; Li J; Zhu Y; Qiu H; Pan J; Wang R; Qian S; Xu W; Xue Y
Exp Oncol; 2007 Dec; 29(4):299-303. PubMed ID: 18199987
[TBL] [Abstract][Full Text] [Related]
37. [Clinical and experimental study of two cases of myelodysplastic syndromes with double isochromosome 20q- anomaly].
Gong SL; Xue YQ; Wang JM; Han FL; Xu YQ; Li JY
Zhonghua Xue Ye Xue Za Zhi; 2005 Jan; 26(1):35-8. PubMed ID: 15946507
[TBL] [Abstract][Full Text] [Related]
38. Shwachman-Diamond syndrome: an inherited model of aplastic anaemia with accelerated angiogenesis.
Leung EW; Rujkijyanont P; Beyene J; Wei K; Abdelhaleem M; Freedman MH; Dror Y
Br J Haematol; 2006 Jun; 133(5):558-61. PubMed ID: 16681645
[TBL] [Abstract][Full Text] [Related]
39. FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: implications for formation and pathogenetic outcome of the idic(7)(p11.2).
Schaad K; Strömbeck B; Mandahl N; Andersen MK; Heim S; Mertens F; Johansson B
Cytogenet Genome Res; 2006; 114(2):126-30. PubMed ID: 16825763
[TBL] [Abstract][Full Text] [Related]
40.
Mourad S; Bilodeau M; Roussy M; Laramée L; Boulianne L; Rouette A; Jouan L; Gendron P; Duval M; Teira P; Hébert J; Bittencourt H; Pastore Y; Landry JR; Cellot S
Front Oncol; 2019; 9():772. PubMed ID: 31475115
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
