Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomes
- 1 January 1992
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 88 (3) , 279-282
- https://doi.org/10.1007/bf00197259
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Recurrence risk of a new dominant mutation in children of unaffected parents.1991
- Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locusCell, 1990
- Parental origin of mutations of the retinoblastoma geneNature, 1989
- MULTIPOINT LINKAGE ANALYSIS IN NEUROFIBROMATOSIS TYPE-I - AN INTERNATIONAL COLLABORATION1989
- IDENTIFICATION OF MORE THAN 500 RFLPS BY SCREENING RANDOM GENOMIC CLONES1988
- Genetic analysis of NF1: Identification of close flanking markers on chromosome 17Genomics, 1987
- Linkage studies with chromosome 17 DNA markers in 45 neurofibromatosis 1 familiesGenomics, 1987
- Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17Science, 1987
- The pathophysiology of neurofibromatosis: IX. Paternal age as a factor in the origin of new mutationsAmerican Journal of Medical Genetics, 1984
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983