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Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines.
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Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11Q deletion in tumors lacking MYCN amplification.
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Chromosomal aberrations in Bloom syndrome patients with myeloid malignancies.
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Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein-methyltransferase superfamily.
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Multicentre analysis of patterns of DNA gains and losses in 204 neuroblastoma tumors: How many genetic subgroups are there?
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Genetica en kanker: perspectieven voor diagnose en behandeling.
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Deletion mapping on the short arm of chromosome 1 in Merkel cell carcinoma.
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Mutation analysis of P73 and TP53 in Merkel cell carcinoma.
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Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects.
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An integrated 5-Mb physical, genetic, and radiation hybrid map of a 1p36.1 region implicated in neuroblastoma pathogenesis.