Rossi M, Laduca J, Cowell J, Srivastava B, Matsui S
Leuk Res. 2007; 32(3):455-63.
PMID: 17640729
PMC: 2855542.
DOI: 10.1016/j.leukres.2007.04.019.
Thiagalingam S, Laken S, WILLSON J, Markowitz S, Kinzler K, Vogelstein B
Proc Natl Acad Sci U S A. 2001; 98(5):2698-702.
PMID: 11226302
PMC: 30201.
DOI: 10.1073/pnas.051625398.
Stasi R, Taylor C, Venditti A, Del Poeta G, Aronica G, Bastianelli C
Ann Hematol. 1995; 71(1):13-27.
PMID: 7632814
DOI: 10.1007/BF01696228.
Kozak C, Sears J, HOGGAN M
J Virol. 1983; 47(1):217-20.
PMID: 6864883
PMC: 255231.
DOI: 10.1128/JVI.47.1.217-220.1983.
Lambert B, Holmberg K, Einhorn N
Hum Genet. 1984; 67(1):94-8.
PMID: 6745931
DOI: 10.1007/BF00270564.
Genetic change in the cancer cell.
HARNDEN D
Br J Cancer. 1984; 49(1):1-3.
PMID: 6691894
PMC: 1976670.
DOI: 10.1038/bjc.1984.1.
A new oncogene, c-raf, is located on mouse chromosome 6.
Kozak C, Gunnell M, Rapp U
J Virol. 1984; 49(1):297-9.
PMID: 6690719
PMC: 255459.
DOI: 10.1128/JVI.49.1.297-299.1984.
Localisation of the human N-ras oncogene to chromosome 1cen - p21 by in situ hybridisation.
Davis M, Malcolm S, Hall A, Marshall C
EMBO J. 1983; 2(12):2281-3.
PMID: 6667677
PMC: 555446.
DOI: 10.1002/j.1460-2075.1983.tb01735.x.
Molecular cloning of the c-fms locus and its assignment to human chromosome 5.
Roussel M, Sherr C, Barker P, Ruddle F
J Virol. 1983; 48(3):770-3.
PMID: 6632085
PMC: 255409.
DOI: 10.1128/JVI.48.3.770-773.1983.
Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: verification by standard staining techniques, new densitometric methods, and somatic cell hybridization.
Squire J, Phillips R, Boyce S, Godbout R, Rogers B, Gallie B
Hum Genet. 1984; 66(1):46-53.
PMID: 6583158
DOI: 10.1007/BF00275185.
Chromosomal assignment of a family of human oncogenes.
Ryan J, Barker P, Shimizu K, Wigler M, Ruddle F
Proc Natl Acad Sci U S A. 1983; 80(14):4460-3.
PMID: 6576347
PMC: 384058.
DOI: 10.1073/pnas.80.14.4460.
Clinical DNA flow cytometry.
Tribukait B
Med Oncol Tumor Pharmacother. 1984; 1(4):211-8.
PMID: 6544901
DOI: 10.1007/BF02934525.
Chromosomes for molecular hybridization. Assignment of repetitive and single copy genes using a rapid filter-fixation method.
Langer G, Blin N, Stoehr M
Histochemistry. 1984; 80(5):469-73.
PMID: 6480413
DOI: 10.1007/BF00495436.
IgG heavy chain allotype (Gm), a genetic marker for human chromosome 14q32, and haematopoietic malignancies.
Nakao Y, Matsumoto H, Tsuji K, Miyazaki T, Masaoka T, Nakayama S
Clin Exp Immunol. 1984; 56(3):628-36.
PMID: 6430611
PMC: 1536010.
Somatic cell fusion as a source of genetic rearrangement leading to metastatic variants.
Larizza L, Schirrmacher V
Cancer Metastasis Rev. 1984; 3(3):193-222.
PMID: 6388823
DOI: 10.1007/BF00048385.
Human oncogenes.
Willecke K, Schafer R
Hum Genet. 1984; 66(2-3):132-42.
PMID: 6370829
DOI: 10.1007/BF00286587.
Correlation between tumorigenicity and banding pattern of chromosome 15 in murine T-cell leukemia cells and hybrids of normal and malignant cells.
Somssich I, Spira J, Hameister H, Klein G
Chromosoma. 1984; 91(1):39-45.
PMID: 6335425
DOI: 10.1007/BF00286483.
Telomeric association of chromosomes in B-cell lymphoid leukemia.
Fitzgerald P, Morris C
Hum Genet. 1984; 67(4):385-90.
PMID: 6333380
DOI: 10.1007/BF00291396.
Cellular DNA region involved in induction of thymic lymphomas (Mlvi-2) maps to mouse chromosome 15.
Tsichlis P, STRAUSS P, Kozak C
Mol Cell Biol. 1984; 4(5):997-1000.
PMID: 6328284
PMC: 368860.
DOI: 10.1128/mcb.4.5.997-1000.1984.
Regional localization of two human cellular Kirsten ras genes on chromosomes 6 and 12.
Sakaguchi A, Zabel B, Grzeschik K, Law M, Ellis R, Scolnick E
Mol Cell Biol. 1984; 4(5):989-93.
PMID: 6328282
PMC: 368856.
DOI: 10.1128/mcb.4.5.989-993.1984.