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L T Sharpe

Showing results (51-60 of 56) with videos related to

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Neuron|January 7, 2000
Color signals in human motion-selective cortexB A Wandell, A B Poirson, W T Newsome, et al.
Investigative Ophthalmology & Visual Science|June 8, 1999
Direct visual resolution of gene copy number in the human photopigment gene arrayS Wolf, L T Sharpe, H J Schmidt, et al.
Human Molecular Genetics|August 25, 2000
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21S Kohl, B Baumann, M Broghammer, et al.
American Journal of Human Genetics|November 1, 1993
Genetic heterogeneity among blue-cone monochromatsJ Nathans, I H Maumenee, E Zrenner, et al.
Genomics|August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11B Wissinger, H Jägle, S Kohl, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Neuron|January 7, 2000
Color signals in human motion-selective cortexB A Wandell, A B Poirson, W T Newsome, et al.
Investigative Ophthalmology & Visual Science|June 8, 1999
Direct visual resolution of gene copy number in the human photopigment gene arrayS Wolf, L T Sharpe, H J Schmidt, et al.
Human Molecular Genetics|August 25, 2000
Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21S Kohl, B Baumann, M Broghammer, et al.
American Journal of Human Genetics|November 1, 1993
Genetic heterogeneity among blue-cone monochromatsJ Nathans, I H Maumenee, E Zrenner, et al.
Genomics|August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11B Wissinger, H Jägle, S Kohl, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Pageof 6