Authors:
Kitamura, E
Kuemerle, BA
Chernova, OB
Cowell, JK
Citation: E. Kitamura et al., Molecular characterization of the breakpoint region associated with a constitutional t(2;15)(q34;q26) in a patient with multiple myeloma, CANC GENET, 129(2), 2001, pp. 112-119
Authors:
Lahti-Domenici, J
Rapakko, K
Paakkonen, K
Allinen, M
Nevanlinna, H
Kujala, M
Huusko, P
Winqvist, R
Citation: J. Lahti-domenici et al., Exclusion of large deletions and other rearrangements in BRCA1 and BRCA2 in Finnish breast and ovarian cancer families, CANC GENET, 129(2), 2001, pp. 120-123
Citation: Jl. Schwartz et al., Characteristics of chromosome instability in the human lymphoblast cell line WTK1, CANC GENET, 129(2), 2001, pp. 124-130
Authors:
Cao, Q
Abeysinghe, H
Chow, O
Xu, J
Kaung, HL
Fong, CT
Keng, P
Insel, RA
Lee, WCM
Barrett, JC
Wang, N
Citation: Q. Cao et al., Suppression of tumorigenicity in human ovarian carcinoma cell line SKOV-3 by microcell-mediated transfer of chromosome 11, CANC GENET, 129(2), 2001, pp. 131-137
Authors:
Sambani, C
Trafalis, DTP
Mitsoulis-Mentzikoff, C
Poulakidas, E
Makropoulos, V
Pantelias, GE
Mecucci, C
Citation: C. Sambani et al., Clonal chromosome rearrangements in hairy cell leukemia: personal experience and review of literature, CANC GENET, 129(2), 2001, pp. 138-144
Authors:
Hoff, C
Mollenhauer, J
Waldau, B
Hamann, U
Poustka, A
Citation: C. Hoff et al., Allelic imbalance and fine mapping of the 17p13.3 subregion in sporadic breast carcinomas, CANC GENET, 129(2), 2001, pp. 145-149
Citation: Ji. Dickstein et al., Localization of the chromosome 22 breakpoints in two cases of acute megakaryoblastic leukemia with t(1;22)(p13;q13), CANC GENET, 129(2), 2001, pp. 150-154
Authors:
Cherry, AM
Bangs, CD
Jones, P
Hall, S
Natkunam, Y
Citation: Am. Cherry et al., A unique AML1 (CBF2A) rearrangement, t(1;21)(p32;q22), observed in a patient with acute myelomonocytic leukemia, CANC GENET, 129(2), 2001, pp. 155-160
Citation: I. Lemke et al., Large deletion of part of the HMGIC locus accompanying a t(3;12)(q27 similar to q28;q14 similar to q15) in a lipoma, CANC GENET, 129(2), 2001, pp. 161-164
Authors:
Smith, A
Robson, L
St Heaps, L
Sharma, P
Dunlop, L
Bhave, A
Bradstock, K
Citation: A. Smith et al., Routine fluorescence in situ hybridization with the MLL probe does not reliably detect two separate signals on one chromosome 11 in patients with trisomy 11, CANC GENET, 129(2), 2001, pp. 173-176
Authors:
Tamura, A
Miura, I
Iida, S
Yokota, S
Horiike, S
Nishida, K
Fujii, H
Nakamura, S
Seto, M
Ueda, R
Taniwaki, M
Citation: A. Tamura et al., Interphase detection of immunoglobulin heavy chain gene translocations with specific oncogene loci in 173 patients with B-cell lymphoma, CANC GENET, 129(1), 2001, pp. 1-9
Authors:
Kim, GJ
Park, SY
Kim, H
Chun, YH
Park, SH
Citation: Gj. Kim et al., Chromosomal aberrations in neuroblastoma cell lines identified by cross species color banding and chromosome painting, CANC GENET, 129(1), 2001, pp. 10-16
Authors:
Cheng, LR
Ramesh, KH
Radel, E
Ratech, H
Wei, DM
Cannizzaro, LA
Citation: Lr. Cheng et al., Characterization of t(11;19)(q23;p13.3) by fluorescence in situ hybridization analysis in a pediatric patient with therapy-related acute myelogenous leukemia, CANC GENET, 129(1), 2001, pp. 17-22
Authors:
Pribill, I
Speiser, P
Leary, J
Leodolter, S
Hacker, NF
Friedlander, ML
Birnbaum, D
Zeillinger, R
Krainer, M
Citation: I. Pribill et al., High frequency of allelic imbalance at regions of chromosome arm 8p in ovarian carcinoma, CANC GENET, 129(1), 2001, pp. 23-29
Authors:
Okubo, M
Tsurukubo, Y
Higaki, T
Kawabe, T
Goto, M
Murase, T
Ide, T
Furuichi, Y
Sugimoto, M
Citation: M. Okubo et al., Clonal chromosomal aberrations accompanied by strong telomerase activity in immortalization of human B-lymphoblastoid cell lines transformed by Epstein-Barr virus, CANC GENET, 129(1), 2001, pp. 30-34
Authors:
Herbst, LH
Chakrabarti, R
Klein, PA
Achary, M
Citation: Lh. Herbst et al., Differential gene expression associated with tumorigenicity of cultured green turtle fibropapilloma-derived fibroblasts, CANC GENET, 129(1), 2001, pp. 35-39
Authors:
Tommasi, S
Abatangelo, M
Lacalamita, R
Montemurro, S
Marzullo, F
Paradiso, A
Citation: S. Tommasi et al., Mutations spanning P53 exons 5-9 detected by non-isotopic RNAse cleavage assay and protein expression in human colon cancer, CANC GENET, 129(1), 2001, pp. 40-42
Citation: M. Yagci et al., Therapy-related refractory anemia with ringed sideroblasts in chronic lymphocytic leukemia: involvement of 3q21 region, CANC GENET, 129(1), 2001, pp. 43-46
Authors:
Kirchhoff, M
Rose, H
Petersen, BL
Maahr, J
Gerdes, T
Philip, J
Lundsteen, C
Citation: M. Kirchhoff et al., Comparative genomic hybridization reveals non-random chromosomal aberrations in early preinvasive cervical lesions, CANC GENET, 129(1), 2001, pp. 47-51
Authors:
Hashimoto, Y
Oga, A
Kawauchi, S
Furuya, T
Shimizu, N
Nakano, T
Imate, Y
Yamashita, H
Sasaki, K
Citation: Y. Hashimoto et al., Amplification of 3q26 similar to qter correlates with tumor progression inhead and neck squamous cell carcinomas, CANC GENET, 129(1), 2001, pp. 52-56