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G A Nicholson

Showing results (41-50 of 115) with videos related to

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International Journal of Surgery (London, England)|March 19, 2015
Augmenting the decision making process in acute appendicitis: A retrospective cohort studyM A Abdelhalim, J D A Stuart, G A Nicholson
Neuroscience|March 18, 2004
Evidence that a major site of expression of the RHO-GTPASE activating protein, oligophrenin-1, is peripheral myelinJ Xiao, C B Neylon, G A Nicholson, et al.
The Medical Journal of Australia|April 20, 1992
Antenatal testing for Charcot-Marie-Tooth neuropathyG A Nicholson, M Kennerson, G Morgan, et al.
American 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.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1994
Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindredJ A Frith, J G McLeod, G A Nicholson, 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.
American Journal of Human Genetics|May 1, 1988
Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type IL R Griffiths, M B Zwi, J G McLeod, et al.
Lancet (London, England)|March 31, 1979
Carrier detection in Duchenne muscular dystrophy: Assessment of the effect of age on detection-rate with serum-creatine-kinase-activityG A Nicholson, D Gardner-Medwin, R J Pennington, et al.
Clinical Chemistry|October 1, 1995
Single test for two hereditary neuropathies, CMT1A and HNPPM L Kennerson, M J Gordon, I P Blair, et al.
Journal of the Neurological Sciences|July 1, 1981
Carrier testing in families of isolated cases of duchenne muscular dystrophy. Creatine kinase activities in female relatives of mothers with normal CK activityG A Nicholson, R J Lane, D Gardner-Medwin, et al.
Pageof 12

Showing results (41-50 of 115) with videos related to

Sort By:
Pageof 12
International Journal of Surgery (London, England)|March 19, 2015
Augmenting the decision making process in acute appendicitis: A retrospective cohort studyM A Abdelhalim, J D A Stuart, G A Nicholson
Neuroscience|March 18, 2004
Evidence that a major site of expression of the RHO-GTPASE activating protein, oligophrenin-1, is peripheral myelinJ Xiao, C B Neylon, G A Nicholson, et al.
The Medical Journal of Australia|April 20, 1992
Antenatal testing for Charcot-Marie-Tooth neuropathyG A Nicholson, M Kennerson, G Morgan, et al.
American 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.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1994
Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindredJ A Frith, J G McLeod, G A Nicholson, 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.
American Journal of Human Genetics|May 1, 1988
Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type IL R Griffiths, M B Zwi, J G McLeod, et al.
Lancet (London, England)|March 31, 1979
Carrier detection in Duchenne muscular dystrophy: Assessment of the effect of age on detection-rate with serum-creatine-kinase-activityG A Nicholson, D Gardner-Medwin, R J Pennington, et al.
Clinical Chemistry|October 1, 1995
Single test for two hereditary neuropathies, CMT1A and HNPPM L Kennerson, M J Gordon, I P Blair, et al.
Journal of the Neurological Sciences|July 1, 1981
Carrier testing in families of isolated cases of duchenne muscular dystrophy. Creatine kinase activities in female relatives of mothers with normal CK activityG A Nicholson, R J Lane, D Gardner-Medwin, et al.
Pageof 12