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Cytogenetics and Cell Genetics|January 1, 1997
Fine mapping of the hereditary sensory neuropathy type I locus on chromosome 9q22.1-->q22.3: exclusion of GAS1 and XPAI P Blair, J L Dawkins, G A NicholsonClinical Chemistry|August 1, 1995
Detection of Charcot-Marie-Tooth type 1A duplication by the polymerase chain reactionI P Blair, M L Kennerson, G A NicholsonCurrent Molecular Medicine|September 10, 2011
Molecular genetics and mechanisms of disease in distal hereditary motor neuropathies: insights directing future genetic studiesA P Drew, I P Blair, G A NicholsonAmerican Journal of Human Genetics|March 1, 1996
Prevalence and origin of de novo duplications in Charcot-Marie-Tooth disease type 1A: first report of a de novo duplication with a maternal originI P Blair, J Nash, M J Gordon, et al.Genomics|September 2, 1998
A YAC-based transcript map of human chromosome 9q22.1-q22.3 encompassing the loci for hereditary sensory neuropathy type I and multiple self-healing squamous epitheliomaI P Blair, D Hulme, J L Dawkins, et al.Human Genetics|August 15, 2000
Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysisD J Hulme, I P Blair, J L Dawkins, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 30, 2009
A novel TARDBP mutation in an Australian amyotrophic lateral sclerosis kindredK L Williams, J C Durnall, A D Thoeng, et al.American Journal of Human Genetics|August 2, 2001
Hereditary sensory neuropathy type I: haplotype analysis shows founders in southern England and EuropeG A Nicholson, J L Dawkins, I P Blair, et al.Nature Genetics|May 1, 1996
The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3G A Nicholson, J L Dawkins, I P Blair, et al.Neurology|May 5, 1998
Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophyP A Silburn, G A Nicholson, B T Teh, et al.Pageof 2