110 related articles for article (PubMed ID: 11156446)
1. Chromosome 7 heteromorphism.
Mark HF
Cancer Genet Cytogenet; 2000 Dec; 123(2):144. PubMed ID: 11156446
[No Abstract] [Full Text] [Related]
2. Spurious monosomy 7 in leukemia due to centromeric heteromorphism.
Duval A; Feneux D; Sutton L; Tchernia G; Léonard C
Cancer Genet Cytogenet; 2000 May; 119(1):67-9. PubMed ID: 10812174
[TBL] [Abstract][Full Text] [Related]
3. Detection of unexpected clones of monosomy 7 in childhood acute lymphoblastic leukemia using fluorescence in situ hybridization.
Kadam P; Masterson M; Soukup S; Moore C; Raza A; Lampkin BC
Anticancer Res; 1994; 14(2A):545-8. PubMed ID: 8017858
[TBL] [Abstract][Full Text] [Related]
4. Acquired centromeric heteromorphism of chromosome 7 yields discordant results between fluorescent in situ hybridization and karyotype analysis in a child with severe congenital neutropenia.
Farra C; Raimondi S; Abboud M
Pediatr Hematol Oncol; 2019 Oct; 36(7):432-437. PubMed ID: 31411529
[TBL] [Abstract][Full Text] [Related]
5. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
6. High-density genome array is superior to fluorescence in-situ hybridization analysis of monosomy 3 in choroidal melanoma fine needle aspiration biopsy.
Young TA; Burgess BL; Rao NP; Gorin MB; Straatsma BR
Mol Vis; 2007 Dec; 13():2328-33. PubMed ID: 18199974
[TBL] [Abstract][Full Text] [Related]
7. Prognostic significance of monosomal karyotype in higher risk myelodysplastic syndrome treated with azacitidine.
Itzykson R; Thépot S; Eclache V; Quesnel B; Dreyfus F; Beyne-Rauzy O; Turlure P; Vey N; Recher C; Boehrer S; Gardin C; Adès L; Fenaux P;
Leukemia; 2011 Jul; 25(7):1207-9. PubMed ID: 21468040
[No Abstract] [Full Text] [Related]
8. Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia.
Sokolic RA; Ferguson W; Mark HF
Cancer Genet Cytogenet; 1999 Dec; 115(2):106-13. PubMed ID: 10598142
[TBL] [Abstract][Full Text] [Related]
9. Raji revisited: cytogenetics of the original Burkitt's lymphoma cell line.
Karpova MB; Schoumans J; Ernberg I; Henter JI; Nordenskjöld M; Fadeel B
Leukemia; 2005 Jan; 19(1):159-61. PubMed ID: 15457187
[No Abstract] [Full Text] [Related]
10. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
Zunino A; Viaggi S; Ottaggio L; Fronza G; Schenone A; Roncella S; Abbondandolo A
Haematologica; 2000 Mar; 85(3):250-5. PubMed ID: 10702812
[TBL] [Abstract][Full Text] [Related]
11. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
Kato R; Kishibayashi J; Shimokawa O; Harada N; Niikawa N; Matsumoto N
Am J Med Genet; 2001 Dec; 104(4):319-22. PubMed ID: 11754068
[TBL] [Abstract][Full Text] [Related]
12. [Interphasic in situ fluorescent hybridization (FISH) in 4 cases of myeloid neoplasias with chromosome 7 changes].
Arranz E; Renedo M; Ramos C; Martínez B; Prieto E; Benítez J
Sangre (Barc); 1994 Dec; 39(6):457-60. PubMed ID: 7855698
[TBL] [Abstract][Full Text] [Related]
13. Der(16)t(1;16)(q10;p10) in multiple myeloma: a new non-random abnormality that is frequently associated with Burkitt's-type translocations.
Mugneret F; Sidaner I; Favre B; Manone L; Maynadié M; Caillot D; Solary E
Leukemia; 1995 Feb; 9(2):277-81. PubMed ID: 7869764
[TBL] [Abstract][Full Text] [Related]
14. Williams-Beuren Syndrome and Burkitt Leukemia.
Zhukova N; Naqvi A
J Pediatr Hematol Oncol; 2013 Jan; 35(1):e30-2. PubMed ID: 23018576
[TBL] [Abstract][Full Text] [Related]
15. [Detection of monosomy 7 or 7q- in cases of myelodysplastic syndrome].
Shen Y; Xue Y; Li J; Guo Y; Pan J; Wu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Aug; 18(4):255-8. PubMed ID: 11484160
[TBL] [Abstract][Full Text] [Related]
16. Sequential karyotyping in Burkitt lymphoma reveals a linear clonal evolution with increase in karyotype complexity and a high frequency of recurrent secondary aberrations.
Aukema SM; Theil L; Rohde M; Bauer B; Bradtke J; Burkhardt B; Bonn BR; Claviez A; Gattenlöhner S; Makarova O; Nagel I; Oschlies I; Pott C; Szczepanowski M; Traulsen A; Kluin PM; Klapper W; Siebert R; Murga Penas EM
Br J Haematol; 2015 Sep; 170(6):814-25. PubMed ID: 26104998
[TBL] [Abstract][Full Text] [Related]
17. Burkitt lymphoma with a duplication of der(8)t(2;8). Interpretation of a complex karyotype by chromosome painting.
Vázquez-Mazariego Y; Cabello P; García-Sagredo JM; López-Yarto A; Vallcorba I; Resino M; Muñoz R; Pérez I; Mayayo M; Ferro MT
Cancer Genet Cytogenet; 1994 Sep; 76(2):136-9. PubMed ID: 7923063
[TBL] [Abstract][Full Text] [Related]
18. Sequential chronic myelogenous leukemia, B-lineage lymphoma and erythroleukemia with monosomy 7 over 10 years.
Au WY; Wan TS; Leung RY; Lie AK
Leuk Lymphoma; 2012 Apr; 53(4):733-5. PubMed ID: 21958131
[No Abstract] [Full Text] [Related]
19. Mapping of MYC breakpoints in 8q24 rearrangements involving non-immunoglobulin partners in B-cell lymphomas.
Bertrand P; Bastard C; Maingonnat C; Jardin F; Maisonneuve C; Courel MN; Ruminy P; Picquenot JM; Tilly H
Leukemia; 2007 Mar; 21(3):515-23. PubMed ID: 17230227
[TBL] [Abstract][Full Text] [Related]
20. Burkitt lymphoma with dual translocation of chromosome 14: a novel chromosomal abnormality of t(8;14),t(14;15).
Moon Y; Kim M; Park G
Ann Clin Lab Sci; 2008; 38(1):75-9. PubMed ID: 18316785
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]