134 related articles for article (PubMed ID: 9305599)
1. Unbalanced t(3;12) in a case of juvenile myelomonocytic leukemia (JMML) results in partial trisomy of 3q as defined by FISH.
Tosi S; Mosna G; Cazzaniga G; Giudici G; Kearney L; Biondi A; Privitera E
Leukemia; 1997 Sep; 11(9):1465-8. PubMed ID: 9305599
[TBL] [Abstract][Full Text] [Related]
2. TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13).
Wlodarska I; Mecucci C; Marynen P; Guo C; Franckx D; La Starza R; Aventin A; Bosly A; Martelli MF; Cassiman JJ
Blood; 1995 May; 85(10):2848-52. PubMed ID: 7742547
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy of 3q detected by chromosome painting in a case of juvenile chronic myelomonocytic leukemia.
Michalová K; Bartsch O; Starý J; Jelínek J; Wiegant J; Bubanská E
Cancer Genet Cytogenet; 1993 Nov; 71(1):67-70. PubMed ID: 8275454
[TBL] [Abstract][Full Text] [Related]
4. A new breakpoint, telomeric to TEL/ETV6, on the short arm of chromosome 12 in T cell acute lymphoblastic leukemia.
Le Coniat M; Della Valle V; Marynen P; Berger R
Leukemia; 1997 Aug; 11(8):1360-3. PubMed ID: 9264392
[TBL] [Abstract][Full Text] [Related]
5. Two unbalanced translocations, t(12;22)(p13;q11) and t(12;?)(p13;?), in an aggressive chronic B-cell leukemia: TEL gene analysis using FISH.
Conchon M; McManus AP; Min T; Maljaie SH; Crawford A; Brito-Babapulle V; Matutes E; Catovsky D
Cancer Genet Cytogenet; 1997 Jun; 95(2):137-40. PubMed ID: 9169030
[TBL] [Abstract][Full Text] [Related]
6. Translocation (8;12)(q13;p13) during disease progression in acute myelomonocytic leukemia with t(11;19)(q23;p13.1).
Yamamoto K; Nagata K; Tsurukubo Y; Inagaki K; Ono R; Taki T; Hayashi Y; Hamaguchi H
Cancer Genet Cytogenet; 2002 Aug; 137(1):64-7. PubMed ID: 12377416
[TBL] [Abstract][Full Text] [Related]
7. Chromosome abnormalities of the short arm of chromosome 12 in hematopoietic malignancies: a report including three novel translocations involving the TEL/ETV6 gene.
Berger R; Le Coniat M; Lacronique V; Daniel MT; Lessard M; Berthou C; Marynen P; Bernard O
Leukemia; 1997 Sep; 11(9):1400-3. PubMed ID: 9305591
[TBL] [Abstract][Full Text] [Related]
8. Characterization of a t(10;12)(q24;p13) in a case of CML in transformation.
Aguiar RC; Chase A; Oscier DG; Carapeti M; Goldman JM; Cross NC
Genes Chromosomes Cancer; 1997 Dec; 20(4):408-11. PubMed ID: 9408758
[TBL] [Abstract][Full Text] [Related]
9. ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia.
Cavé H; Cacheux V; Raynaud S; Brunie G; Bakkus M; Cochaux P; Preudhomme C; Laï JL; Vilmer E; Grandchamp B
Leukemia; 1997 Sep; 11(9):1459-64. PubMed ID: 9305598
[TBL] [Abstract][Full Text] [Related]
10. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.
Murga Penas EM; Cools J; Algenstaedt P; Hinz K; Seeger D; Schafhausen P; Schilling G; Marynen P; Hossfeld DK; Dierlamm J
Genes Chromosomes Cancer; 2003 May; 37(1):79-83. PubMed ID: 12661008
[TBL] [Abstract][Full Text] [Related]
11. Translocation (12;22) (p13;q11) in myeloproliferative disorders results in fusion of the ETS-like TEL gene on 12p13 to the MN1 gene on 22q11.
Buijs A; Sherr S; van Baal S; van Bezouw S; van der Plas D; Geurts van Kessel A; Riegman P; Lekanne Deprez R; Zwarthoff E; Hagemeijer A
Oncogene; 1995 Apr; 10(8):1511-9. PubMed ID: 7731705
[TBL] [Abstract][Full Text] [Related]
12. Abnormalities of the ETV6 gene occur in the majority of patients with aberrations of the short arm of chromosome 12: a combined PCR and Southern blotting analysis.
O'Connor HE; Butler TA; Clark R; Swanton S; Harrison CJ; Secker-Walker LM; Foroni L
Leukemia; 1998 Jul; 12(7):1099-106. PubMed ID: 9665196
[TBL] [Abstract][Full Text] [Related]
13. Interstitial deletion of the short arm of chromosome 12 during clonal evolution in myelodysplastic syndrome with t(5;12)(q13;p13) involving the ETV6 gene.
Yamamoto K; Nagata K; Yagasaki F; Tsurukubo Y; Tamura A; Taniwaki M; Hamaguchi H
Cancer Genet Cytogenet; 2000 Jun; 119(2):113-7. PubMed ID: 10867145
[TBL] [Abstract][Full Text] [Related]
14. Cryptic t(12;15)(p13;q26) producing the ETV6-NTRK3 fusion gene and no loss of IGF2 imprinting in congenital mesoblastic nephroma with trisomy 11: fluorescence in situ hybridization and IGF2 allelic expression analysis.
Watanabe N; Kobayashi H; Hirama T; Kikuta A; Koizumi S; Tsuru T; Kaneko Y
Cancer Genet Cytogenet; 2002 Jul; 136(1):10-6. PubMed ID: 12165445
[TBL] [Abstract][Full Text] [Related]
15. Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.
Wieczorek D; Engels H; Viersbach R; Henke B; Schwanitz G; Passarge E
J Med Genet; 1998 Jul; 35(7):545-53. PubMed ID: 9678698
[TBL] [Abstract][Full Text] [Related]
16. Mixed Phenotype Acute Leukemia with t(12;17)(p13;q21)/TAF15-ZNF384 and Other Chromosome Abnormalities.
Yamamoto K; Kawamoto S; Mizutani Y; Yakushijin K; Yamashita T; Nakamachi Y; Kawano S; Hayashi Y; Matsuoka H; Minami H
Cytogenet Genome Res; 2016; 149(3):165-170. PubMed ID: 27607436
[TBL] [Abstract][Full Text] [Related]
17. Molecular cytogenetic characterization of rearrangements involving 12p in leukemia.
Vieira L; Marques B; Cavaleiro C; Ambrósio AP; Jorge M; Neto A; Costa JM; Júnior EC; Boavida MG
Cancer Genet Cytogenet; 2005 Mar; 157(2):134-9. PubMed ID: 15721634
[TBL] [Abstract][Full Text] [Related]
18. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
Balci S; Aypar E; Beksaç MS; Bartsch O
Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
[TBL] [Abstract][Full Text] [Related]
19. Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome.
Jotterand Bellomo M; Parlier V; Mühlematter D; Grob JP; Beris P
Cancer Genet Cytogenet; 1992 Apr; 59(2):138-60. PubMed ID: 1581880
[TBL] [Abstract][Full Text] [Related]
20. Cytogenetic and molecular delineation of a region of chromosome 3q commonly gained in marginal zone B-cell lymphoma.
Gazzo S; Baseggio L; Coignet L; Poncet C; Morel D; Coiffier B; Felman P; Berger F; Salles G; Callet-Bauchu E
Haematologica; 2003 Jan; 88(1):31-8. PubMed ID: 12551824
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
