181 related articles for article (PubMed ID: 11943348)
1. Trisomy 4 as the sole cytogenetic abnormality in a Waldenström macroglobulinemia.
Rivera AI; Li MM; Beltran G; Krause JR
Cancer Genet Cytogenet; 2002 Mar; 133(2):172-3. PubMed ID: 11943348
[TBL] [Abstract][Full Text] [Related]
2. Chromosomal aberrations and their prognostic value in a series of 174 untreated patients with Waldenström's macroglobulinemia.
Nguyen-Khac F; Lambert J; Chapiro E; Grelier A; Mould S; Barin C; Daudignon A; Gachard N; Struski S; Henry C; Penther D; Mossafa H; Andrieux J; Eclache V; Bilhou-Nabera C; Luquet I; Terre C; Baranger L; Mugneret F; Chiesa J; Mozziconacci MJ; Callet-Bauchu E; Veronese L; Blons H; Owen R; Lejeune J; Chevret S; Merle-Beral H; Leblondon V; ; ;
Haematologica; 2013 Apr; 98(4):649-54. PubMed ID: 23065509
[TBL] [Abstract][Full Text] [Related]
3. A case of t(8;14) with total and partial trisomy 3 in Waldenstrom macroglobulinemia.
Chong YY; Lau LC; Lui WO; Lim P; Lim E; Tan PH; Tan P; Ong YY
Cancer Genet Cytogenet; 1998 May; 103(1):65-7. PubMed ID: 9595048
[TBL] [Abstract][Full Text] [Related]
4. [Gene mutations connected to Waldenstöm macroglobulinemia].
Kutálková K; Sedlaříková L; Adam Z; Ševčíková S
Vnitr Lek; 2016 Jan; 62(1):40-3. PubMed ID: 26967235
[TBL] [Abstract][Full Text] [Related]
5. [Chromosomal abnormalities and Waldenström macroglobulinemia].
Berger R; Nguyen-Khac F
Pathol Biol (Paris); 2008 Sep; 56(6):400-6. PubMed ID: 18456427
[TBL] [Abstract][Full Text] [Related]
6. Concomitant partial tetrasomy 3q and trisomy 18 in Waldenström macroglobulinemia.
Wong KF; Kwong YL; Wong TK
Cancer Genet Cytogenet; 1995 May; 81(1):92-3. PubMed ID: 7773966
[TBL] [Abstract][Full Text] [Related]
7. Cytogenetic findings in lymphoplasmacytic lymphoma/Waldenström macroglobulinemia. Chromosomal abnormalities are associated with the polymorphous subtype and an aggressive clinical course.
Mansoor A; Medeiros LJ; Weber DM; Alexanian R; Hayes K; Jones D; Lai R; Glassman A; Bueso-Ramos CE
Am J Clin Pathol; 2001 Oct; 116(4):543-9. PubMed ID: 11601139
[TBL] [Abstract][Full Text] [Related]
8. Trisomy 4, a new chromosomal abnormality in Waldenström's macroglobulinemia: a study of 39 cases.
Terré C; Nguyen-Khac F; Barin C; Mozziconacci MJ; Eclache V; Léonard C; Chapiro E; Farhat H; Bouyon A; Rousselot P; Choquet S; Spentchian M; Dubreuil P; Leblond V; Castaigne S
Leukemia; 2006 Sep; 20(9):1634-6. PubMed ID: 16838026
[No Abstract] [Full Text] [Related]
9. Clonal chromosome abnormalities in patients with Waldenström's and CLL-associated macroglobulinemia: significance of trisomy 12.
Han T; Sadamori N; Takeuchi J; Ozer H; Henderson ES; Bhargava A; Fitzpatrick J; Sandberg AA
Blood; 1983 Sep; 62(3):525-31. PubMed ID: 6411149
[TBL] [Abstract][Full Text] [Related]
10. Lymphoplasmacytic lymphoma/Waldenström macroglobulinemia with inv(16)(p13q22) as a sole genetic abnormality.
Frater JL; Mirkhaef M; Batanian JR
Cancer Genet Cytogenet; 2007 Apr; 174(2):161-5. PubMed ID: 17452259
[TBL] [Abstract][Full Text] [Related]
11. Isochromosome (6p) in Waldenstrom's macroglobulinemia.
White AD; Clark RE; Jacobs A
Cancer Genet Cytogenet; 1992 Jan; 58(1):89-91. PubMed ID: 1728957
[TBL] [Abstract][Full Text] [Related]
12. Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia.
Bang SM; Seo JW; Park KU; Kim SJ; Kim K; Kim SH; Cho SR; Kim HC; Song J; Kim JS; Kim KH; Lee JH; Lee JJ; Shin MG; Suh C; Chi HS; Oh DY; Won JH; Kim HJ; Yoon SS; Lee DS;
Cancer Genet Cytogenet; 2010 Mar; 197(2):117-21. PubMed ID: 20193844
[TBL] [Abstract][Full Text] [Related]
13. Deletion (20q) as the sole abnormality in Waldenström macroglobulinemia suggests distinct pathogenesis of 20q11 anomaly.
Liu YC; Miyazawa K; Sashida G; Kodama A; Ohyashiki K
Cancer Genet Cytogenet; 2006 Aug; 169(1):69-72. PubMed ID: 16875940
[TBL] [Abstract][Full Text] [Related]
14. Interstitial deletion of 20q in a patient with Waldenström macroglobulinemia following chemotherapy.
Blann MM; Velagaleti GV; Morgan DL; Martinez RE; Conlin PA; Tonk VS
Cancer Genet Cytogenet; 2002 Jan; 132(2):145-8. PubMed ID: 11850077
[TBL] [Abstract][Full Text] [Related]
15. t(1:14) and trisomy 4 in a patient with concomitant leukaemias.
Zahir MN; Masood N; Shabbir-Moosajee M
J Pak Med Assoc; 2014 May; 64(5):596-8. PubMed ID: 25272555
[TBL] [Abstract][Full Text] [Related]
16. Myelodysplastic syndrome with complex karyotypic abnormality in a patient with Waldenström's macroglobulinemia after sequential treatment with chlorambucil and fludarabine.
Shin SJ; Chun SH; Kim KO; Kim MK; Lee KH; Hyun MS; Cho HS
Jpn J Clin Oncol; 2005 Oct; 35(10):622-5. PubMed ID: 16172172
[TBL] [Abstract][Full Text] [Related]
17. [Characteristics of chromosomal complexes in patients with narrow-band (monoclonal) gammapathies (literature survey)].
Zakharova AV
Probl Gematol Pereliv Krovi; 1975 Feb; 20(2):53-62. PubMed ID: 810791
[No Abstract] [Full Text] [Related]
18. [Molecular basis of Waldenström macroglobulinemia].
Sevčíková S; Novák L; Kubiczková L; Dementyeva E; Ríhová L; Hájek R
Klin Onkol; 2012; 25(6):413-20. PubMed ID: 23301642
[TBL] [Abstract][Full Text] [Related]
19. Chromosomal abnormalities in Waldenström's macroglobulinemia.
Carbone P; Caradonna F; Granata G; Marcenò R; Cavallaro AM; Barbata G
Cancer Genet Cytogenet; 1992 Jul; 61(2):147-51. PubMed ID: 1638495
[TBL] [Abstract][Full Text] [Related]
20. Waldenström's macroglobulinemia with the AML/MDS-associated t(1;3)(p36;q21).
Johansson B; Waldenström J; Hasselblom S; Mitelman F
Leukemia; 1995 Jul; 9(7):1136-8. PubMed ID: 7630185
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
