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R F Mullins

Showing results (21-30 of 24) with videos related to

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Human Mutation|May 12, 2009
Predicting the pathogenicity of RPE65 mutationsA R Philp, M Jin, S Li, et al.
Gene Therapy|May 9, 2014
CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotypeE 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 headA 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 1FK N Alagramam, H Yuan, M H Kuehn, et al.
Pageof 3

Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 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 mutationsA R Philp, M Jin, S Li, et al.
Gene Therapy|May 9, 2014
CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotypeE 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 headA 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 1FK N Alagramam, H Yuan, M H Kuehn, et al.
Pageof 3