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G A Nicholson

Showing results (31-40 of 115) with videos related to

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Australian Paediatric Journal|January 1, 1988
DNA probes in Charcot-Marie-Tooth neuropathyG A Nicholson, L R Griffiths, J G McLeod
Australian and New Zealand Journal of Ophthalmology|November 1, 1985
An evaluation of signs in ocular myasthenia gravis and correlation with acetylcholine receptor antibodiesI C Francis, G A Nicholson, M B Kappagoda
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 Nicholson
Pediatrics|August 1, 1977
Screening for Duchenne muscular dystrophyA D Roses, G A Nicholson, C R Roe
Journal of the Neurological Sciences|April 1, 1984
A study of platelet protein phosphorylation in Duchenne muscular dystrophy. Further evidence against the generalised membrane defect theoryG A Nicholson, J G McLeod, J W Sugars
The Medical Journal of Australia|October 1, 1983
Acetylcholine receptor antibody in the diagnosis of myasthenia gravisG A Nicholson, J G McLeod, L R Griffiths
Burns, Including Thermal Injury|March 1, 1983
Myeloneuropathy due to nitrous oxideP J Hayden, R J Hartemink, G A Nicholson
Current 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 Nicholson
Genomics|October 27, 1998
Genomic structure and physical mapping of C17orf1: a gene associated with the proximal element of the CMT1A-REP binary repeatM L Kennerson, N T Nassif, G A Nicholson
Genetic Testing|July 30, 2003
A rapid and definitive test for Charcot-Marie-Tooth 1A and hereditary neuropathy with liability to pressure palsies using multiplexed real-time PCRP Lorentzos, T Kaiser, M L Kennerson, et al.
Pageof 12

Showing results (31-40 of 115) with videos related to

Sort By:
Pageof 12
Australian Paediatric Journal|January 1, 1988
DNA probes in Charcot-Marie-Tooth neuropathyG A Nicholson, L R Griffiths, J G McLeod
Australian and New Zealand Journal of Ophthalmology|November 1, 1985
An evaluation of signs in ocular myasthenia gravis and correlation with acetylcholine receptor antibodiesI C Francis, G A Nicholson, M B Kappagoda
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 Nicholson
Pediatrics|August 1, 1977
Screening for Duchenne muscular dystrophyA D Roses, G A Nicholson, C R Roe
Journal of the Neurological Sciences|April 1, 1984
A study of platelet protein phosphorylation in Duchenne muscular dystrophy. Further evidence against the generalised membrane defect theoryG A Nicholson, J G McLeod, J W Sugars
The Medical Journal of Australia|October 1, 1983
Acetylcholine receptor antibody in the diagnosis of myasthenia gravisG A Nicholson, J G McLeod, L R Griffiths
Burns, Including Thermal Injury|March 1, 1983
Myeloneuropathy due to nitrous oxideP J Hayden, R J Hartemink, G A Nicholson
Current 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 Nicholson
Genomics|October 27, 1998
Genomic structure and physical mapping of C17orf1: a gene associated with the proximal element of the CMT1A-REP binary repeatM L Kennerson, N T Nassif, G A Nicholson
Genetic Testing|July 30, 2003
A rapid and definitive test for Charcot-Marie-Tooth 1A and hereditary neuropathy with liability to pressure palsies using multiplexed real-time PCRP Lorentzos, T Kaiser, M L Kennerson, et al.
Pageof 12