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Science (New York, N.Y.)
|
November 3, 1995
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy
S Noguchi, E M McNally, K Ben Othmane, et al.
Annals of Neurology
|
June 14, 2000
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations
I Nishino, A Spinazzola, A Papadimitriou, et al.
Neurology
|
June 11, 2003
Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype
T Takahashi, M Aoki, M Tateyama, et al.
Page
of 51
Search research articles
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Showing results (501-510 of 503) with videos related to
Sort By:
Page
of 51
You have reached the last page of results.
This site can display upto 503 results.
Science (New York, N.Y.)
|
November 3, 1995
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy
S Noguchi, E M McNally, K Ben Othmane, et al.
Annals of Neurology
|
June 14, 2000
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations
I Nishino, A Spinazzola, A Papadimitriou, et al.
Neurology
|
June 11, 2003
Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype
T Takahashi, M Aoki, M Tateyama, et al.
Page
of 51