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C Inglehearn

Showing results (11-20 of 15) with videos related to

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Human Molecular Genetics|January 1, 1994
A 150 bp insertion in the rhodopsin gene of an autosomal dominant retinitis pigmentosa familyM al-Maghtheh, R Y Kim, A Hardcastle, et al.
Nature Genetics|March 1, 1993
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophyJ Wells, J Wroblewski, J Keen, et al.
The British Journal of Ophthalmology|January 1, 1995
Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expressionR Y Kim, F W Fitzke, A T Moore, et al.
Nature Genetics|February 1, 1994
Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortionK Evans, A Fryer, C Inglehearn, et al.
Ophthalmology|January 1, 1994
Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow geneJ J Wroblewski, J A Wells, A Eckstein, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Human Molecular Genetics|January 1, 1994
A 150 bp insertion in the rhodopsin gene of an autosomal dominant retinitis pigmentosa familyM al-Maghtheh, R Y Kim, A Hardcastle, et al.
Nature Genetics|March 1, 1993
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophyJ Wells, J Wroblewski, J Keen, et al.
The British Journal of Ophthalmology|January 1, 1995
Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expressionR Y Kim, F W Fitzke, A T Moore, et al.
Nature Genetics|February 1, 1994
Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortionK Evans, A Fryer, C Inglehearn, et al.
Ophthalmology|January 1, 1994
Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow geneJ J Wroblewski, J A Wells, A Eckstein, et al.
Pageof 2