Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)
- 1 January 1998
- journal article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 100 (1), 10-20
- https://doi.org/10.1016/s0165-4608(97)00013-7
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Molecular characterization of a (1;10)(p22;q21) constitutional translocation from a patient with neuroblastomaCancer Genetics and Cytogenetics, 1995
- Sensitive detection of numerical and structural aberrations of chromosome 1 in neuroblastoma by interphase fluorescence in situ hybridization. comparison with restriction fragment length polymorphism and conventional cytogenetic analysesInternational Journal of Cancer, 1995
- Chromosomal analysis of two neuroblastomasCancer Genetics and Cytogenetics, 1993
- A 3.5 genome equivalent multi access YAC library: construction, characterisation, screening and storageNucleic Acids Research, 1990
- A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clonesNucleic Acids Research, 1990
- Genetic and Cytogenetic Analysis of Patients Showing Reduced Esterase-D Levels and Mental Retardation from a Survey of 500 Individuals with RetinoblastomaOphthalmic Paediatrics and Genetics, 1989
- The international incidence of childhood cancerInternational Journal of Cancer, 1988
- Tumour karyotype discriminates between good and bad prognostic outcome in neuroblastomaBritish Journal of Cancer, 1988
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983
- Deletions of Chromosome 15 as a Cause of the Prader–Willi SyndromeNew England Journal of Medicine, 1981