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Brain : a Journal of Neurology
|
May 18, 2011
Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skin
Michaela Auer-Grumbach, Martin Weger, Regina Fink-Puches, et al.
American Journal of Human Genetics
|
January 4, 2011
Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I
Christian Guelly, Peng-Peng Zhu, Lea Leonardis, et al.
Blood
|
November 20, 2014
Epigenetic and in vivo comparison of diverse MSC sources reveals an endochondral signature for human hematopoietic niche formation
Andreas Reinisch, Nathalie Etchart, Daniel Thomas, 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.
Brain : a Journal of Neurology
|
May 18, 2011
Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skin
Michaela Auer-Grumbach, Martin Weger, Regina Fink-Puches, et al.
American Journal of Human Genetics
|
January 4, 2011
Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I
Christian Guelly, Peng-Peng Zhu, Lea Leonardis, et al.
Blood
|
November 20, 2014
Epigenetic and in vivo comparison of diverse MSC sources reveals an endochondral signature for human hematopoietic niche formation
Andreas Reinisch, Nathalie Etchart, Daniel Thomas, et al.
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of 6