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American Journal of Human Genetics
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January 13, 2000
De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10
S M van der Maarel, G Deidda, R J Lemmers, et al.
Nature Genetics
|
November 13, 2001
Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter
P A Leegwater, G Vermeulen, A A Könst, et al.
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of 2
Search research articles
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Showing results (11-20 of 12) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 12 results.
American Journal of Human Genetics
|
January 13, 2000
De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10
S M van der Maarel, G Deidda, R J Lemmers, et al.
Nature Genetics
|
November 13, 2001
Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter
P A Leegwater, G Vermeulen, A A Könst, et al.
Page
of 2