Search research articles
Contact Us
Filters
Showing results (21-30 of 24) with videos related to
Page
of 3
Sort By:
You have reached the last page of results.
This site can display upto 24 results.
Human Mutation
|
May 12, 2009
Predicting the pathogenicity of RPE65 mutations
A R Philp, M Jin, S Li, et al.
Gene Therapy
|
May 9, 2014
CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype
E R Burnight, L A Wiley, A V Drack, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 10, 2001
Expression of the glaucoma gene myocilin (MYOC) in the human optic nerve head
A F Clark, K Kawase, S English-Wright, et al.
Human Molecular Genetics
|
August 7, 2001
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
K N Alagramam, H Yuan, M H Kuehn, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 24) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 24 results.
Human Mutation
|
May 12, 2009
Predicting the pathogenicity of RPE65 mutations
A R Philp, M Jin, S Li, et al.
Gene Therapy
|
May 9, 2014
CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype
E R Burnight, L A Wiley, A V Drack, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 10, 2001
Expression of the glaucoma gene myocilin (MYOC) in the human optic nerve head
A F Clark, K Kawase, S English-Wright, et al.
Human Molecular Genetics
|
August 7, 2001
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
K N Alagramam, H Yuan, M H Kuehn, et al.
Page
of 3