Found: 15
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Identification of germline missense mutations and rare allelic variants in the ATM gene in early-onset breast cancer.
- Published in:
- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 286, doi. 10.1002/(SICI)1098-2264(199912)26:4<286::AID-GCC2>3.0.CO;2-X
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Fine-structure deletion mapping of 10q22-24 identifies regions of loss of heterozygosity and suggests that sporadic follicular thyroid adenomas and follicular thyroid carcinomas develop along distinct neoplastic pathways.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 322, doi. 10.1002/(SICI)1098-2264(199912)26:4<322::AID-GCC6>3.0.CO;2-#
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Rapid and sensitive minimal residual disease detection in acute leukemia by quantitative real-time RT-PCR exemplified by t(12;21) TEL-AML1 fusion transcript.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 355, doi. 10.1002/(SICI)1098-2264(199912)26:4<355::AID-GCC10>3.0.CO;2-3
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- Article
Genes, chromosomes, and rhabdomyosarcoma.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 275, doi. 10.1002/(SICI)1098-2264(199912)26:4<275::AID-GCC1>3.0.CO;2-3
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Splice variant lacking the transactivation domain of the BRCA2 gene and mutations in the splice acceptor site of intron 2.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 381, doi. 10.1002/(SICI)1098-2264(199912)26:4<381::AID-GCC14>3.0.CO;2-N
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- Article
Germline mutations in NF1 patients with malignancies.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 376, doi. 10.1002/(SICI)1098-2264(199912)26:4<376::AID-GCC13>3.0.CO;2-O
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Genetic alterations during the progression of squamous cell carcinomas of the uterine cervix.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 346, doi. 10.1002/(SICI)1098-2264(199912)26:4<346::AID-GCC9>3.0.CO;2-D
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Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 312, doi. 10.1002/(SICI)1098-2264(199912)26:4<312::AID-GCC5>3.0.CO;2-3
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- Article
Primary Parauterine Leiomyoma With a t(6;14).
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 385, doi. 10.1002/(SICI)1098-2264(199912)26:4<385::AID-GCC15>3.0.CO;2-G
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- Article
Nonrandom karyotypic features in squamous cell carcinomas of the skin.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 295, doi. 10.1002/(SICI)1098-2264(199912)26:4<295::AID-GCC3>3.0.CO;2-W
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Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 336, doi. 10.1002/(SICI)1098-2264(199912)26:4<336::AID-GCC8>3.0.CO;2-H
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- Article
Missense and nonsense mutations in codon 659 of MLH1 cause aberrant splicing of messenger RNA in HNPCC kindreds.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 372, doi. 10.1002/(SICI)1098-2264(199912)26:4<372::AID-GCC12>3.0.CO;2-V
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- Article
Dominant genetic alterations in immortalization: Role for 20q gain.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 304, doi. 10.1002/(SICI)1098-2264(199912)26:4<304::AID-GCC4>3.0.CO;2-1
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- Article
3′ BCR recombines with IGL locus in BCR-ABL-positive Philadelphia-negative chronic myeloid leukemia.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 366, doi. 10.1002/(SICI)1098-2264(199912)26:4<366::AID-GCC11>3.0.CO;2-X
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Isolation and characterization of a novel TP53-inducible gene, TP53TG3.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 4, p. 329, doi. 10.1002/(SICI)1098-2264(199912)26:4<329::AID-GCC7>3.0.CO;2-C
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- Article