Found: 14
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Narrowing of the region of allelic loss in 21q11-21 in squamous non-small cell lung carcinoma and cloning of a novel ubiquitin-specific protease gene from the deleted segment.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 153, doi. 10.1002/(SICI)1098-2264(200002)27:2<153::AID-GCC6>3.0.CO;2-A
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Comparison between genotype and phenotype identifies a high-risk population carrying BRCA1 mutations.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 130, doi. 10.1002/(SICI)1098-2264(200002)27:2<130::AID-GCC3>3.0.CO;2-U
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Comparative genomic hybridization analysis of hepatoblastomas.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 196, doi. 10.1002/(SICI)1098-2264(200002)27:2<196::AID-GCC12>3.0.CO;2-D
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Prevalence of germline truncating mutations in ATM in women with a second breast cancer after radiation therapy for a contralateral tumor.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 124, doi. 10.1002/(SICI)1098-2264(200002)27:2<124::AID-GCC2>3.0.CO;2-M
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Molecular genetic alterations in carcinoma ex-pleomorphic adenoma: A putative progression model?
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 162, doi. 10.1002/(SICI)1098-2264(200002)27:2<162::AID-GCC7>3.0.CO;2-9
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Malignant fibrous histiocytoma: Inherited and sporadic forms have loss of heterozygosity at chromosome bands 9p21-22-evidence for a common genetic defect.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 191, doi. 10.1002/(SICI)1098-2264(200002)27:2<191::AID-GCC11>3.0.CO;2-L
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Culture of cytogenetically abnormal Schwann cells from benign and malignant NF1 tumors.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 117, doi. 10.1002/(SICI)1098-2264(200002)27:2<117::AID-GCC1>3.0.CO;2-H
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An integrated 5-Mb physical, genetic, and radiation hybrid map of a 1p36.1 region implicated in neuroblastoma pathogenesis.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 143, doi. 10.1002/(SICI)1098-2264(200002)27:2<143::AID-GCC5>3.0.CO;2-E
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Mutation of BAX occurs infrequently in acquired immunodeficiency syndrome-related non-Hodgkin's lymphomas.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 177, doi. 10.1002/(SICI)1098-2264(200002)27:2<177::AID-GCC9>3.0.CO;2-O
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Centrosome amplification and instability occurs exclusively in aneuploid, but not in diploid colorectal cancer cell lines, and correlates with numerical chromosomal aberrations.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 183, doi. 10.1002/(SICI)1098-2264(200002)27:2<183::AID-GCC10>3.0.CO;2-P
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Dysregulation of HMGIC in a uterine lipoleiomyoma with a complex rearrangement including chromosomes 7, 12, and 14.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 209, doi. 10.1002/(SICI)1098-2264(200002)27:2<209::AID-GCC14>3.0.CO;2-U
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Granulocytic sarcomas in body cavities in childhood acute myeloid leukemias with 11q23/ MLL rearrangements.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 136, doi. 10.1002/(SICI)1098-2264(200002)27:2<136::AID-GCC4>3.0.CO;2-9
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Isolation and mutational analysis of a novel human cDNA, DEC1 (deleted in esophageal cancer 1), derived from the tumor suppressor locus in 9q32.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 169, doi. 10.1002/(SICI)1098-2264(200002)27:2<169::AID-GCC8>3.0.CO;2-M
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Somatic mutations of the APC, KRAS, and TP53 genes in nonpolypoid colorectal adenomas.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 2, p. 202, doi. 10.1002/(SICI)1098-2264(200002)27:2<202::AID-GCC13>3.0.CO;2-3
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