DNA deletion associated with hereditary neuropathy with liability to pressure palsies
- 1 January 1993
- Vol. 72 (1) , 143-151
- https://doi.org/10.1016/0092-8674(93)90058-x
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Viral integration and fragile sites in human papillomavirus‐lmmortalized human keratinocyte cell linesGenes, Chromosomes and Cancer, 1992
- De-novo mutation in hereditary motor and sensory neuropathy type IThe Lancet, 1992
- Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2Genomics, 1991
- A genetic map of human chromosome 17pGenomics, 1990
- Characterization of eight VNTR loci by agarose gel electrophoresisGenomics, 1989
- Long Lives for Homozygous Trembler Mutant Mice Despite Virtual Absence of Peripheral Nerve MyelinScience, 1988
- Status of the linkage map of the mouseCytogenetic and Genome Research, 1978
- Abnormal myelination in transplanted Trembler mouse Schwann cellsNature, 1977
- RECURRENT BRACHIAL PLEXUS NEUROPATHYBrain, 1975
- RECURRENT PERIPHERAL-NERVE PALSIES IN A FAMILYThe Lancet, 1954