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E M Stone

Showing results (141-150 of 174) with videos related to

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Human Molecular Genetics|September 1, 1997
Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpointR Y Walder, H Shalev, T M Brennan, et al.
Experimental Eye Research|February 5, 2002
Concentric retinitis pigmentosa: clinicopathologic correlationsA H Milam, E B De Castro, J E Smith, et al.
Investigative Ophthalmology & Visual Science|January 3, 2001
Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertensionJ H Fingert, A F Clark, J E Craig, et al.
Experimental Eye Research|May 11, 2019
Molecular characterization of foveal versus peripheral human retina by single-cell RNA sequencingA P Voigt, S S Whitmore, M J Flamme-Wiese, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.
Human Molecular Genetics|March 1, 1995
Linkage of posterior polymorphous corneal dystrophy to 20q11E Héon, W D Mathers, W L Alward, et al.
The British Journal of Ophthalmology|November 21, 2007
ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathyM Michaelides, L L Chen, M A Brantley, et al.
Nature Genetics|January 1, 1994
Three autosomal dominant corneal dystrophies map to chromosome 5qE M Stone, W D Mathers, G O Rosenwasser, et al.
Nature Genetics|June 10, 1998
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25D Y Nishimura, R E Swiderski, W L Alward, et al.
Pageof 18

Showing results (141-150 of 174) with videos related to

Sort By:
Pageof 18
Human Molecular Genetics|September 1, 1997
Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpointR Y Walder, H Shalev, T M Brennan, et al.
Experimental Eye Research|February 5, 2002
Concentric retinitis pigmentosa: clinicopathologic correlationsA H Milam, E B De Castro, J E Smith, et al.
Investigative Ophthalmology & Visual Science|January 3, 2001
Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertensionJ H Fingert, A F Clark, J E Craig, et al.
Experimental Eye Research|May 11, 2019
Molecular characterization of foveal versus peripheral human retina by single-cell RNA sequencingA P Voigt, S S Whitmore, M J Flamme-Wiese, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.
Human Molecular Genetics|March 1, 1995
Linkage of posterior polymorphous corneal dystrophy to 20q11E Héon, W D Mathers, W L Alward, et al.
The British Journal of Ophthalmology|November 21, 2007
ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathyM Michaelides, L L Chen, M A Brantley, et al.
Nature Genetics|January 1, 1994
Three autosomal dominant corneal dystrophies map to chromosome 5qE M Stone, W D Mathers, G O Rosenwasser, et al.
Nature Genetics|June 10, 1998
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25D Y Nishimura, R E Swiderski, W L Alward, et al.
Pageof 18