Works matching IS 10452257 AND DT 2001 AND VI 31 AND IP 1
Results: 13
Color bar coding the BRCA1 gene on combed DNA: A useful strategy for detecting large gene rearrangements.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 75, doi. 10.1002/gcc.1120
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- Article
Genetic imbalances in 26 cases of penile squamous cell carcinoma.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 48, doi. 10.1002/gcc.1117
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Integration of amplified BCR/ABL fusion genes into the short arm of chromosome 17 as a novel mechanism of disease progression in chronic myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 10, doi. 10.1002/gcc.1112
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- Article
Identification of extensive genomic loss and gain by comparative genomic hybridisation in malignant astrocytoma in children and young adults.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 15, doi. 10.1002/gcc.1113
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- Article
Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 42, doi. 10.1002/gcc.1116
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- Article
Molecular cytogenetic characterization of early and late renal cell carcinomas in Von Hippel-Lindau disease.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 1, doi. 10.1002/gcc.1111
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- Article
Apparent human BRCA1 knockout caused by mispriming during polymerase chain reaction: Implications for genetic testing.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 96, doi. 10.1002/gcc.1122
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- Article
Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 33, doi. 10.1002/gcc.1115
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A classification efficiency test of spectral karyotyping and multiplex fluorescence in situ hybridization: Identification of chromosome homologies between Homo sapiens and Hylobates leucogenys.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 65, doi. 10.1002/gcc.1119
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A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: A possible role of the Alu-polyA tail in the evolution of the deletion.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 91, doi. 10.1002/gcc.1110
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ALK probe rearrangement in a t(2;11; 2)(p23;p15; q31) translocation found in a prenatal myofibroblastic fibrous lesion: Toward a molecular definition of an inflammatory myofibroblastic tumor family?
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 85, doi. 10.1002/gcc.1121
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- Article
Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15).
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 23, doi. 10.1002/gcc.1114
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Characterization of chromosome aberrations associated with soft-tissue leiomyosarcomas by twenty-four-color karyotyping and comparative genomic hybridization analysis.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 1, p. 54, doi. 10.1002/gcc.1118
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- Article