Works matching IS 10452257 AND DT 1996 AND VI 15 AND IP 3
Results: 12
Have cancer cytogeneticists been wrong in assigning chromosome 12 breakpoints in benign tumors?
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 195, doi. 10.1002/1098-2264(199603)15:3<195::AID-GCC2870150302>3.0.CO;2-G
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Retinoic acid regulatory pathways, chromosomal translocations, and acute promyelocytic leukemia.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 147, doi. 10.1002/(SICI)1098-2264(199603)15:3<147::AID-GCC1>3.0.CO;2-2
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Molecular cytogenetic assignment of the chromosome 12 breakpoints in many benign tumors to 12q15 Affecting the HMGIC gene.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 195, doi. 10.1002/1098-2264(199603)15:3<195::AID-GCC2870150303>3.0.CO;2-D
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Identification of a YAC spanning the translocation breakpoint t(8;22) associated with acute monocytic leukemia.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 191, doi. 10.1002/(SICI)1098-2264(199603)15:3<191::AID-GCC9>3.0.CO;2-Y
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Molecular variant of the NPM-ALK rearrangement of Ki-l lymphoma involving a cryptic ALK splice site.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 173, doi. 10.1002/(SICI)1098-2264(199603)15:3<173::AID-GCC5>3.0.CO;2-#
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Cytogenetic analysis of three primary Bellini duct carcinomas.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 170, doi. 10.1002/(SICI)1098-2264(199603)15:3<170::AID-GCC4>3.0.CO;2-#
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Infrequent mutations of the TP53 gene and no amplification of the MDM2 gene in hepatoblastomas.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 187, doi. 10.1002/(SICI)1098-2264(199603)15:3<187::AID-GCC8>3.0.CO;2-Z
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Masthead.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. fmi, doi. 10.1002/1098-2264(199603)15:3<::AID-GCC2870150301>3.0.CO;2-F
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Genetic mechanisms in esophageal carcinogenesis: Frequent deletion of 3p and 17p in premalignant lesions.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 165, doi. 10.1002/(SICI)1098-2264(199603)15:3<165::AID-GCC3>3.0.CO;2-0
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Loss of the chromosomal region 5q11-q31 in the myeloid cell line HL-60: Characterization by comparative genomic hybridization and fluorescence in situ hybridization.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 182, doi. 10.1002/(SICI)1098-2264(199603)15:3<182::AID-GCC7>3.0.CO;2-Z
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Sensitive detection of loss of heterozygosity in the TP53 gene in pancreatic adenocarcinoma by fluorescence-based single-strand conformation polymorphism analysis using blunt-end DNA fragments.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 157, doi. 10.1002/(SICI)1098-2264(199603)15:3<157::AID-GCC2>3.0.CO;2-1
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Clonal chromosome abnormalities in two chemodectomas.
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- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 178, doi. 10.1002/(SICI)1098-2264(199603)15:3<178::AID-GCC6>3.0.CO;2-#
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