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B E Nichols

Showing results (1-10 of 21) with videos related to

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Computer Applications in the Biosciences : CABIOS|December 1, 1993
A user-friendly Hypercard interface for human linkage analysisB E Nichols, V C Sheffield, E M Stone
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|March 1, 1997
Evaluation of a significantly shorter version of the Farnsworth-Munsell 100-hue test in patients with three different optic neuropathiesB E Nichols, H S Thompson, E M Stone
Journal of Internal Medicine|September 21, 2011
HIV testing and antiretroviral treatment strategies for prevention of HIV infection: impact on antiretroviral drug resistanceB E Nichols, C A B Boucher, D A M C van de Vijver
Nature Genetics|July 1, 1992
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13E M Stone, B E Nichols, L M Streb, et al.
American Journal of Human Genetics|January 1, 1994
Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1B E Nichols, R Bascom, M Litt, et al.
Human Molecular Genetics|May 1, 1993
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the foveaB E Nichols, A V Drack, K Vandenburgh, et al.
Nature Genetics|March 1, 1993
Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS geneB E Nichols, V C Sheffield, K Vandenburgh, et al.
Ophthalmology|December 1, 1991
Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin geneE M Stone, A E Kimura, B E Nichols, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1994
Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6qE M Stone, B E Nichols, A E Kimura, et al.
Human Molecular Genetics|August 1, 1993
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the foveaB E Nichols, A V Drack, K Vandenburgh, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Computer Applications in the Biosciences : CABIOS|December 1, 1993
A user-friendly Hypercard interface for human linkage analysisB E Nichols, V C Sheffield, E M Stone
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|March 1, 1997
Evaluation of a significantly shorter version of the Farnsworth-Munsell 100-hue test in patients with three different optic neuropathiesB E Nichols, H S Thompson, E M Stone
Journal of Internal Medicine|September 21, 2011
HIV testing and antiretroviral treatment strategies for prevention of HIV infection: impact on antiretroviral drug resistanceB E Nichols, C A B Boucher, D A M C van de Vijver
Nature Genetics|July 1, 1992
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13E M Stone, B E Nichols, L M Streb, et al.
American Journal of Human Genetics|January 1, 1994
Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1B E Nichols, R Bascom, M Litt, et al.
Human Molecular Genetics|May 1, 1993
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the foveaB E Nichols, A V Drack, K Vandenburgh, et al.
Nature Genetics|March 1, 1993
Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS geneB E Nichols, V C Sheffield, K Vandenburgh, et al.
Ophthalmology|December 1, 1991
Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin geneE M Stone, A E Kimura, B E Nichols, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1994
Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6qE M Stone, B E Nichols, A E Kimura, et al.
Human Molecular Genetics|August 1, 1993
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the foveaB E Nichols, A V Drack, K Vandenburgh, et al.
Pageof 3