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Proceedings of the National Academy of Sciences of the United States of America
|
August 18, 1999
Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina
J Bennett, A M Maguire, A V Cideciyan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
April 15, 2000
Mutation analysis of 3 genes in patients with Leber congenital amaurosis
A J Lotery, P Namperumalsamy, S G Jacobson, et al.
Cell
|
December 9, 1997
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
C L Freund, C Y Gregory-Evans, T Furukawa, et al.
Nature Genetics
|
November 4, 2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
N T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Nature Genetics
|
February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
N B Haider, S G Jacobson, A V Cideciyan, et al.
American Journal of Human Genetics
|
November 4, 2000
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I
L M Astuto, M D Weston, C A Carney, et al.
Nature Genetics
|
May 31, 2001
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4
K Mykytyn, T Braun, R Carmi, et al.
Human Molecular Genetics
|
April 4, 2001
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)
D Y Nishimura, C C Searby, R Carmi, et al.
American Journal of Human Genetics
|
September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disorders
B Wissinger, D Gamer, H Jägle, et al.
Page
of 14
Search research articles
Search
Showing results (131-140 of 139) with videos related to
Sort By:
Page
of 14
You have reached the last page of results.
This site can display upto 139 results.
Proceedings of the National Academy of Sciences of the United States of America
|
August 18, 1999
Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina
J Bennett, A M Maguire, A V Cideciyan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
April 15, 2000
Mutation analysis of 3 genes in patients with Leber congenital amaurosis
A J Lotery, P Namperumalsamy, S G Jacobson, et al.
Cell
|
December 9, 1997
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
C L Freund, C Y Gregory-Evans, T Furukawa, et al.
Nature Genetics
|
November 4, 2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
N T Bech-Hansen, M J Naylor, T A Maybaum, et al.
Nature Genetics
|
February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
N B Haider, S G Jacobson, A V Cideciyan, et al.
American Journal of Human Genetics
|
November 4, 2000
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I
L M Astuto, M D Weston, C A Carney, et al.
Nature Genetics
|
May 31, 2001
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4
K Mykytyn, T Braun, R Carmi, et al.
Human Molecular Genetics
|
April 4, 2001
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)
D Y Nishimura, C C Searby, R Carmi, et al.
American Journal of Human Genetics
|
September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disorders
B Wissinger, D Gamer, H Jägle, et al.
Page
of 14