Genes, Chromosomes and Cancer: Vol 26, No 4

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Genes, Chromosomes and Cancer

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Genes, Chromosomes and Cancer: Volume 26, Issue 4

REVIEW ARTICLES

Genes, chromosomes, and rhabdomyosarcoma

RESEARCH ARTICLES

Identification of germline missense mutations and rare allelic variants in the ATM gene in early-onset breast cancer

Nonrandom karyotypic features in squamous cell carcinomas of the skin

Dominant genetic alterations in immortalization: Role for 20q gain

Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas

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

Isolation and characterization of a novel TP53-inducible gene, TP53TG3

Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome

Genetic alterations during the progression of squamous cell carcinomas of the uterine cervix

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

BRIEF COMMUNICATIONS

3′ BCR recombines with IGL locus in BCR-ABL–positive Philadelphia-negative chronic myeloid leukemia

Missense and nonsense mutations in codon 659 of MLH1 cause aberrant splicing of messenger RNA in HNPCC kindreds

Germline mutations in NF1 patients with malignancies

Letter to the Editors

Splice variant lacking the transactivation domain of the BRCA2 gene and mutations in the splice acceptor site of intron 2

Primary Parauterine Leiomyoma With a t(6;14)

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Genes, Chromosomes and Cancer

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Genes, Chromosomes and Cancer: Volume 26, Issue 4

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REVIEW ARTICLES

Genes, chromosomes, and rhabdomyosarcoma

RESEARCH ARTICLES

Identification of germline missense mutations and rare allelic variants in the ATM gene in early-onset breast cancer

Nonrandom karyotypic features in squamous cell carcinomas of the skin

Dominant genetic alterations in immortalization: Role for 20q gain

Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas

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

Isolation and characterization of a novel TP53-inducible gene, TP53TG3

Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome

Genetic alterations during the progression of squamous cell carcinomas of the uterine cervix

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

BRIEF COMMUNICATIONS

3′ BCR recombines with IGL locus in BCR-ABL–positive Philadelphia-negative chronic myeloid leukemia

Missense and nonsense mutations in codon 659 of MLH1 cause aberrant splicing of messenger RNA in HNPCC kindreds

Germline mutations in NF1 patients with malignancies

Letter to the Editors

Splice variant lacking the transactivation domain of the BRCA2 gene and mutations in the splice acceptor site of intron 2

Primary Parauterine Leiomyoma With a t(6;14)

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