75 related articles for article (PubMed ID: 22157696)
1. Multiple copies of duplicated 1q in myelodysplastic syndrome.
Wong KF; Wong WS
Pathology; 2012 Jan; 44(1):57-8. PubMed ID: 22157696
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluations.
Karaoguz MY; Biri A; Pala E; Kan D; Poyraz A; Kurdoglu M; Percin EF
Genet Couns; 2006; 17(2):197-204. PubMed ID: 16970038
[TBL] [Abstract][Full Text] [Related]
6. Neonatal pancytopenia associated with de novo 1q43-44 deletion and 10p15 duplication.
Treskov I; Al-Hosni M; Havranek T; Batanian J
J Pediatr Hematol Oncol; 2013 Apr; 35(3):e94-9. PubMed ID: 23337548
[TBL] [Abstract][Full Text] [Related]
7. [A 57-year-old patient with peripheral pancytopenia].
Fink M; Prenninger S; Sauer H
Internist (Berl); 1989 Mar; 30(3):210-3. PubMed ID: 2654063
[No Abstract] [Full Text] [Related]
8. Sequential observation of clinical and karyotypic evolution in a patient with myelodysplastic syndrome.
Xue YQ; Guo Y; Lin BJ; Zhang GR; Lu DW; Wang MH; Gu YZ; Gong JX; Wang LX
Chin Med J (Engl); 1989 Sep; 102(9):689-94. PubMed ID: 2517082
[TBL] [Abstract][Full Text] [Related]
9. A special type of chromosome 1 abnormality in myelodysplastic syndrome patients: duplication 1q.
Yu Y; Zhang T; Zeng Z; Wang Q; Hong Y; Shen H; Wu D; Pan J; Chen S; Sun A
Br J Haematol; 2020 Jun; 189(5):e218-e221. PubMed ID: 32301121
[No Abstract] [Full Text] [Related]
10. Myelodysplastic syndrome with hypereosinophilia and a nonrandom chromosomal abnormality dic(1;7): confirmation of eosinophil clonal involvement by fluorescence in situ hybridization.
Forrest DL; Horsman DE; Jensen CL; Berry BR; Dalal BI; Barnett MJ; Nantel SH
Cancer Genet Cytogenet; 1998 Nov; 107(1):65-8. PubMed ID: 9809037
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The association between the myelodysplastic syndromes and Crohn disease.
Eng C; Farraye FA; Shulman LN; Peppercorn MA; Krauss CM; Connors JM; Stone RM
Ann Intern Med; 1992 Oct; 117(8):661-2. PubMed ID: 1530197
[No Abstract] [Full Text] [Related]
13. [Isochromosome 17q as the sole alteration in 2 patients with a myelodysplastic syndrome and its relation to myeloperoxidase activity].
Solé F; Pérez A; Woessner S; Olmedo E; Florensa L; Sans J
Sangre (Barc); 1991 Aug; 36(4):323-5. PubMed ID: 1663663
[TBL] [Abstract][Full Text] [Related]
14. Two cases of myeloid disorders and a t(8;12) (q12;p13).
Hernández JM; González MB; García JL; Ferro MT; Gutiérrez NC; Marynen P; San Miguel JF
Haematologica; 2000 Jan; 85(1):31-4. PubMed ID: 10629588
[TBL] [Abstract][Full Text] [Related]
15. Abnormalities of chromosome 1p/q are highly associated with chromosome 13/13q deletions and are an adverse prognostic factor for the outcome of high-dose chemotherapy in patients with multiple myeloma.
Wu KL; Beverloo B; Lokhorst HM; Segeren CM; van der Holt B; Steijaert MM; Westveer PH; Poddighe PJ; Verhoef GE; Sonneveld P; ;
Br J Haematol; 2007 Feb; 136(4):615-23. PubMed ID: 17223915
[TBL] [Abstract][Full Text] [Related]
16. [Peculiarities of cytogenetic changes in different types of myelodysplastic syndrome].
Lozyns'ka MP; Vyhovs'ka IaI; Tomashevs'ka NIa; Masliak ZV; Lozyns'kyĭ RIu; Novak VL
Tsitol Genet; 2009; 43(1):61-8. PubMed ID: 19663317
[TBL] [Abstract][Full Text] [Related]
17. Gain of 1q in pediatric myelodysplastic syndromes.
Morerio C; Rapella A; Tassano E; Lanino E; Micalizzi C; Rosanda C; Panarello C
Leuk Res; 2006 Nov; 30(11):1437-41. PubMed ID: 16472857
[TBL] [Abstract][Full Text] [Related]
18. Refractory anaemia with hypereosinophilia and clonal abnormal metaphases detected only in the neutrophilic granulopoietic series.
Pérez-Losada A; Woessner S; Solé F; Florensa L; Grañena A
Acta Haematol; 1994; 91(2):80-3. PubMed ID: 8023649
[TBL] [Abstract][Full Text] [Related]
19. [Azathioprine-associated myelodysplastic syndrome with cytogenetic aberrations].
Willerding-Möllmann S; Wilkens L; Schlegelberger B; Kaiser U
Dtsch Med Wochenschr; 2004 May; 129(22):1246-8. PubMed ID: 15170581
[TBL] [Abstract][Full Text] [Related]
20. A new case of myelodysplastic syndrome with 6p rearrangement.
Jotterand-Bellomo M; Parlier V; Petite J; Beris J
Cancer Genet Cytogenet; 1990 Feb; 44(2):271-4. PubMed ID: 2297686
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
