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A constitutional translocation t(1;17)(p36.2;q11.2) in a neuroblastoma patient disrupts the the human NBPF1 and ACCN1 genes
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Small-molecule MDM2 antagonists as a new therapy concept for neuroblastoma
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The von Hippel-Lindau tumor suppressor gene expression level has prognostic value in neuroblastoma
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Translocation-excision-deletion-amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1
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Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type
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Rapid detection of VHL exon deletions using real-time quantitative PCR
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Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type I patients.