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Broberg, K
Domanski, HA
Toksvig-Larsen, S
Lindstrand, A
Mandahl, N
Mertens, F
Citation: A. Dahlen et al., Analysis of the distribution and frequency of trisomy 7 in vivo in synoviafrom patients with osteoarthritis and pigmented villonodular synovitis, CANC GENET, 131(1), 2001, pp. 19-24
Citation: F. Micci et al., Complete cytogenetic characterization of the human breast cancer cell lineMA11 combining G-banding, comparative genomic hybridization, multicolor fluorescence in situ hybridization, RxFISH, and chromosome-specific painting, CANC GENET, 131(1), 2001, pp. 25-30
Authors:
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Bastie, JN
Garcia, I
Suzan, F
Cayuela, JM
Therond, P
Castaigne, S
Citation: C. Terre et al., BCR/ABL fusion gene detected on 9q34 by fluorescence in situ hybridizationin an acute leukemia with two BCR/ABL positive clones, one Ph-negative andone Ph-positive, CANC GENET, 131(1), 2001, pp. 37-41
Authors:
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Shyong, WY
Chang, MS
Chen, YJ
Lin, CH
Huang, ZD
Wang, TY
Hsu, MT
Chen, ML
Citation: Yc. Yang et al., Frequent gain of copy number on the long arm of chromosome 3 in human cervical adenocarcinoma, CANC GENET, 131(1), 2001, pp. 48-53
Authors:
Kitay-Cohen, Y
Amiel, A
Ashur, Y
Fejgin, MD
Herishanu, Y
Afanasyev, F
Bomstein, Y
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Citation: Y. Kitay-cohen et al., Analysis of chromosomal aberrations in large hepatocellular carcinomas by comparative genomic hybridization, CANC GENET, 131(1), 2001, pp. 60-64
Authors:
Yamamoto, K
Nagata, K
Kida, A
Hamaguchi, H
Citation: K. Yamamoto et al., Deletion of 16q11 is a recurrent cytogenetic aberration in acute myeloblastic leukemia during disease progression, CANC GENET, 131(1), 2001, pp. 65-68
Authors:
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Rokman, A
Palmberg, C
Hyytinen, ER
Laurila, M
Tammela, TLJ
Koivisto, PA
Citation: K. Haapala et al., Chromosomal changes in locally recurrent, hormone-refractory prostate carcinomas by karyotyping and comparative genomic hybridization, CANC GENET, 131(1), 2001, pp. 74-78
Authors:
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Chun, K
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Malkin, D
Citation: Pc. Nathan et al., Isochromosome (17)(q10) and translocation (4;12)(q12;p13) in a child with acute myeloid leukemia, CANC GENET, 131(1), 2001, pp. 82-85
Citation: L. Zhao et al., Spectral karyo-typing study of chromosome abnormalities in human leukemia (vol 127, pg 143, 2001), CANC GENET, 131(1), 2001, pp. 94-95
Authors:
Andreasson, P
Schwaller, J
Anastasiadou, E
Aster, J
Gilliland, DG
Citation: P. Andreasson et al., The expression of ETV6/CBFA2 (TEL/AML1) is not sufficient for the transformation of hematopoietic cell lines in vitro or the induction of hematologicdisease in vivo, CANC GENET, 130(2), 2001, pp. 93-104
Authors:
Glukhova, L
Angevin, E
Lavialle, C
Cadot, B
Terrier-Lacombe, MJ
Perbal, B
Bernheim, A
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Citation: L. Glukhova et al., Patterns of specific genomic alterations associated with poor prognosis inhigh-grade renal cell carcinomas, CANC GENET, 130(2), 2001, pp. 105-110
Authors:
Jin, YS
Jin, C
Wennerberg, J
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Mertens, F
Citation: Ys. Jin et al., Cytogenetic and fluorescence in situ hybridization characterization of chromosome 8 rearrangements in head and neck squamous cell carcinomas, CANC GENET, 130(2), 2001, pp. 111-117
Authors:
Eklund, LK
Islam, K
Soderkvist, P
Islam, MQ
Citation: Lk. Eklund et al., Regional mapping of suppressor loci for anchorage independence and tumorigenicity on human chromosome 9, CANC GENET, 130(2), 2001, pp. 118-126
Authors:
Takeo, S
Arai, H
Kusano, N
Harada, T
Furuya, T
Kawauchi, S
Oga, A
Hirano, T
Yoshida, T
Okita, K
Sasaki, K
Citation: S. Takeo et al., Examination of oncogene amplification by genomic DNA microarray in hepatocellular carcinomas: comparison with comparative genomic hybridization analysis, CANC GENET, 130(2), 2001, pp. 127-132
Authors:
McConville, CM
Dyer, S
Rees, SA
Luttikhuis, MEMO
McMullan, DJ
Vickers, SJ
Ramani, P
Redfern, D
Morland, BJ
Citation: Cm. Mcconville et al., Molecular cytogenetic characterization of two non-MYCN amplified neuroblastoma cell lines with complex t(11;17), CANC GENET, 130(2), 2001, pp. 133-140