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Results of search for 'au:"Cherryson, A K"'
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Authors
Bananis, T
Blair, I P
Bolhuis, P A
Bragg, T L
Brown, R H
Cherryson, A K
Chin, W
Dawkins, J L
DeKroon, R M
Dench, J E
Esteban, J
Gordon, M J
Hayward, L J
Horvitz, H R
Hosler, B A
Kennerson, M L
Laing, N G
McLeod, J G
Mckenna-Yasek, D
Nicholson, G A
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Amyotrophic Lateral Sclerosis
Australia
Base Sequence
Chromosome Mapping
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 9
DNA
DNA Primers
Exons
Family
Family Health
Female
Frameshift Mutation
Genetic Linkage
Genetic Markers
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genetics
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Your search returned 3 results.
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1.
The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3.
[electronic resource]
by
Nicholson, G A
Dawkins, J L
Blair, I P
Kennerson, M L
Gordon, M J
Cherryson, A K
Nash, J
Bananis, T
Producer:
19960809
In:
Nature genetics
vol. 13
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Available from publisher's website
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No items available.
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2.
A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies.
[electronic resource]
by
Nicholson, G A
Valentijn, L J
Cherryson, A K
Kennerson, M L
Bragg, T L
DeKroon, R M
Ross, D A
Pollard, J D
McLeod, J G
Bolhuis, P A
Producer:
19940725
In:
Nature genetics
vol. 6
Online resources:
Available from publisher's website
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3.
Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis.
[electronic resource]
by
Hosler, B A
Nicholson, G A
Sapp, P C
Chin, W
Orrell, R W
de Belleroche, J S
Esteban, J
Hayward, L J
Mckenna-Yasek, D
Yeung, L
Cherryson, A K
Dench, J E
Wilton, S D
Laing, N G
Horvitz, H R
Brown, R H
Producer:
19970227
In:
Neuromuscular disorders : NMD
vol. 6
Online resources:
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