Cloning and characterization of the human t(3;6)(p14;p11) translocation breakpoint associated with hematologic malignancies.

[1]  A. Panani,et al.  Cytogenetic studies in preleukaemia using the G-banding staining technique. , 2009, Scandinavian journal of haematology.

[2]  al. et,et al.  Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia , 1993, Science.

[3]  H. Aburatani,et al.  Clinical and Genetic Studies of Renal Cell Carcinomas in a Family with a Constitutional Chromosome 3; 8 Translocation: Genetics of Familial Renal Carcinoma , 1993, Annals of Internal Medicine.

[4]  K. Gardiner,et al.  Analysis of chromosome 21 yeast artificial chromosome (YAC) clones. , 1992, American journal of human genetics.

[5]  K. Tanaka,et al.  Loss of heterozygosity at D3S2 locus of short arm of chromosome 3 in chronic myelogenous leukemia. , 1992, Cancer genetics and cytogenetics.

[6]  P. Green,et al.  Localization of 616 human chromosome 3-specific cosmids using a somatic cell hybrid deletion mapping panel. , 1991, Genomics.

[7]  J. Siegfried,et al.  Chromosome alterations in 21 non‐small cell lung carcinomas , 1990, Genes, chromosomes & cancer.

[8]  H. Drabkin,et al.  Development of a somatic cell hybrid mapping panel and molecular probes for human chromosome 3. , 1990, Genomics.

[9]  J. Minna,et al.  Molecular mapping of deletion sites in the short arm of chromosome 3 in human lung cancer , 1990, Genes, chromosomes & cancer.

[10]  R. Lidereau,et al.  Presence of two members of c-erbA receptor gene family (c-erbA beta and c-erbA2) in smallest region of somatic homozygosity on chromosome 3p21-p25 in human breast carcinoma. , 1989, Journal of the National Cancer Institute.

[11]  P. Devilee,et al.  At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma. , 1989, Genomics.

[12]  D. Ledbetter,et al.  Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[13]  J. Yokota,et al.  Loss of heterozygosity on the short arm of chromosome 3 in carcinoma of the uterine cervix. , 1989, Cancer research.

[14]  D. Schlessinger,et al.  Isolation of single-copy human genes from a library of yeast artificial chromosome clones. , 1989, Science.

[15]  J. Haines,et al.  Von Hippel–Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma , 1988, Nature.

[16]  G. Klein,et al.  Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[17]  H. Brauch,et al.  Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma , 1988, Nature.

[18]  J. Minna,et al.  Molecular analysis of the short arm of chromosome 3 in small-cell and non-small-cell carcinoma of the lung. , 1987, The New England journal of medicine.

[19]  M. Olson,et al.  Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors. , 1987, Science.

[20]  K. Franssila,et al.  Constitutional translocation t(3;6)(p14;p11) in a family with hematologic malignancies. , 1987, Cancer genetics and cytogenetics.

[21]  J. Yunis The chromosomal basis of human neoplasia. , 1983, Science.

[22]  A. Feinberg,et al.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.

[23]  D. Patterson,et al.  Structural gene coding for multifunctional protein carrying orotate phosphoribosyltransferase and OMP decarboxylase activity is located on long arm of human chromosome 3 , 1983, Somatic cell genetics.

[24]  J. Minna,et al.  Specific chromosome defect associated with human small-cell lung cancer; deletion 3p(14-23). , 1982, Science.

[25]  E. Southern Detection of specific sequences among DNA fragments separated by gel electrophoresis. , 1975, Journal of molecular biology.

[26]  G. Kovacs,et al.  Nonhomologous chromatid exchange in hereditary and sporadic renal cell carcinomas. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[27]  G. Chu Pulsed field electrophoresis in contour‐clamped homogeneous electric fields for the resolution of DNA by size or topology , 1989, Electrophoresis.

[28]  J. Minna,et al.  Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer , 1987, Nature.