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PAX5/IGH rearrangement is a recurrent finding in a subset of aggressive B‐NHL with complex chromosomal rearrangementsThis text presents research results of the Belgian program of Interuniversity Poles of Attraction initiated by the Belgian State, Prime Minister's Office, Science Policy Programming. The scientific responsibility is assumed by the authors.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 218, doi. 10.1002/gcc.20214
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Molecular and immunohistochemical investigation of protein kinase a regulatory subunit type 1A (PRKAR1A) in odontogenic myxomasThis article is a US Government work and, as such, is in the public domain in the United States of America.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 204
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Delineation of distinct subgroups of multiple myeloma and a model for clonal evolution based on interphase cytogenetics.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 194, doi. 10.1002/gcc.20231
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Identification of individual genes altered in squamous cell carcinoma of the vulva.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 185, doi. 10.1002/gcc.20230
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Nonrandom cell‐cycle timing of a somatic chromosomal translocation: The t(X;17) of alveolar soft‐part sarcoma occurs in G2.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 170, doi. 10.1002/gcc.20229
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- Article
Nitrosamine 4‐(methylnitrosamino)‐1‐(3‐pyridyl)‐1‐butanone‐induced pulmonary adenocarcinomas in Syrian golden hamsters contain beta 2‐adrenergic receptor single‐nucleotide polymorphisms.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 212, doi. 10.1002/gcc.20228
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Cytogenetic evaluation of a large series of hepatoblastomas: Numerical abnormalities with recurring aberrations involving 1q12–q21.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 177, doi. 10.1002/gcc.20227
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Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3).
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 154
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Chromosome 22 tiling‐path array–CGH analysis identifies germ‐line‐ and tumor‐specific aberrations in patients with glioblastoma multiforme.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 161
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Evidence for a single‐step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 113, doi. 10.1002/gcc.20222
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Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC).
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 123, doi. 10.1002/gcc.20219
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Oncogene amplification in the proximal part of chromosome 6 in rat endometrial adenocarcinoma as revealed by combined BAC/PAC FISH, chromosome painting, zoo‐FISH, and allelotyping.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 2, p. 139, doi. 10.1002/gcc.20220
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