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American Journal of Human Genetics
|
April 21, 2009
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease
Andrew J Duncan, Maria Bitner-Glindzicz, Brigitte Meunier, et al.
L'Encephale
|
January 10, 2021
[Towards better management for sexual offenders: Presentation and conclusions of a public hearing concerning prevention, assessment, and care]
S Mouchet-Mages, C Alezrah, S Allag-Morris, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 21, 2007
The implications of alternative splicing in the ENCODE protein complement
Michael L Tress, Pier Luigi Martelli, Adam Frankish, et al.
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of 6
Search research articles
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Showing results (51-60 of 53) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 53 results.
American Journal of Human Genetics
|
April 21, 2009
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease
Andrew J Duncan, Maria Bitner-Glindzicz, Brigitte Meunier, et al.
L'Encephale
|
January 10, 2021
[Towards better management for sexual offenders: Presentation and conclusions of a public hearing concerning prevention, assessment, and care]
S Mouchet-Mages, C Alezrah, S Allag-Morris, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 21, 2007
The implications of alternative splicing in the ENCODE protein complement
Michael L Tress, Pier Luigi Martelli, Adam Frankish, et al.
Page
of 6