Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell line
- 1 December 1992
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 90 (4) , 450-456
- https://doi.org/10.1007/bf00220476
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- NF is enough of GAPNature, 1992
- Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patientsNature, 1992
- cDNA cloning of the type 1 neurofibromatosis gene: Complete sequence of the NF1 gene productGenomics, 1991
- Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.Proceedings of the National Academy of Sciences, 1990
- Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locusCell, 1990
- Mutations in the p53 gene occur in diverse human tumour typesNature, 1989
- Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA.Proceedings of the National Academy of Sciences, 1989
- Genetic analysis of NF1: Identification of close flanking markers on chromosome 17Genomics, 1987
- The gene for human p53 cellular tumor antigen is located on chromosome 17 short arm (17p13).Proceedings of the National Academy of Sciences, 1986
- Polymorphic DNA region adjacent to the 5' end of the human insulin gene.Proceedings of the National Academy of Sciences, 1981