Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease
- 1 August 1990
- journal article
- case report
- Published by Springer Nature in Human Genetics
- Vol. 85 (3) , 337-342
- https://doi.org/10.1007/bf00206758
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Sister chromatid exchanges and chromosome aberrations in von Recklinghausen's disease-a family studyHereditas, 2008
- Neurofibromatosis 2: Clinical and DNA Linkage Studies of a Large KindredNew England Journal of Medicine, 1988
- Neurofibromatosis 2New England Journal of Medicine, 1988
- Linkage of NF1 to 12 chromosome 17 markers: A summary of eight concurrent reportsGenomics, 1987
- Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor genePublished by Elsevier ,1987
- Neurofibromatosis in a man with a ring 22: In situ hybridization studiesCancer Genetics and Cytogenetics, 1987
- Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuromaNature, 1986
- Evidence of chromosomal instability in neurofibromatosisCancer, 1985
- Von Recklinghausen NeurofibromatosisNew England Journal of Medicine, 1981
- THE CHROMOSOMAL FINDINGS IN SEVEN HUMAN NEURINOMAS AND ONE NEUROSARCOMAActa Pathologica Microbiologica Scandinavica Section A Pathology, 1972