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Nature
|
June 2, 1986
The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice
A Dautigny, M G Mattei, D Morello, et al.
European Neurology
|
January 1, 1997
New mutations in the X-linked form of Charcot-Marie-Tooth disease
P Latour, A Fabreguette, C Ressot, et al.
American Journal of Human Genetics
|
September 22, 2001
Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation
D Rodriguez, F Gauthier, E Bertini, et al.
Neurogenetics
|
December 14, 1999
Linkage analysis of candidate myelin genes in familial multiple sclerosis
E Seboun, J R Oksenberg, A Rombos, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 54) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 54 results.
Nature
|
June 2, 1986
The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice
A Dautigny, M G Mattei, D Morello, et al.
European Neurology
|
January 1, 1997
New mutations in the X-linked form of Charcot-Marie-Tooth disease
P Latour, A Fabreguette, C Ressot, et al.
American Journal of Human Genetics
|
September 22, 2001
Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation
D Rodriguez, F Gauthier, E Bertini, et al.
Neurogenetics
|
December 14, 1999
Linkage analysis of candidate myelin genes in familial multiple sclerosis
E Seboun, J R Oksenberg, A Rombos, et al.
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of 6