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E M Stone

Showing results (61-70 of 174) with videos related to

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Carcinogenesis|August 1, 1996
Metabolic activation and DNA binding of food mutagens and other environmental carcinogens in human mammary epithelial cellsP L Carmichael, E M Stone, P L Grover, et al.
Journal of Glaucoma|August 1, 1996
Molecular genetics of glaucoma: current statusW L Alward, A T Johnson, D Y Nishimura, et al.
American Journal of Human Genetics|March 1, 1992
Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, J S Beck, B Nichols, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1997
Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)J Brown, J H Fingert, C M Taylor, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Molecular characterization and ophthalmic investigation of a large family with type 2A Von Hippel-Lindau DiseaseR C Allen, A R Webster, R Sui, et al.
American Journal of Human Genetics|October 1, 1995
Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from IsraelD A Scott, R Carmi, K Elbedour, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 17, 1999
Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR geneG A Fishman, E M Stone, S Grover, 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.
Experimental Eye Research|November 1, 1996
Preferential rod and cone photoreceptor abnormalities in heterozygotes with point mutations in the RDS geneS G Jacobson, A V Cideciyan, A M Maguire, 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.
Pageof 18

Showing results (61-70 of 174) with videos related to

Sort By:
Pageof 18
Carcinogenesis|August 1, 1996
Metabolic activation and DNA binding of food mutagens and other environmental carcinogens in human mammary epithelial cellsP L Carmichael, E M Stone, P L Grover, et al.
Journal of Glaucoma|August 1, 1996
Molecular genetics of glaucoma: current statusW L Alward, A T Johnson, D Y Nishimura, et al.
American Journal of Human Genetics|March 1, 1992
Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, J S Beck, B Nichols, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1997
Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)J Brown, J H Fingert, C M Taylor, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Molecular characterization and ophthalmic investigation of a large family with type 2A Von Hippel-Lindau DiseaseR C Allen, A R Webster, R Sui, et al.
American Journal of Human Genetics|October 1, 1995
Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from IsraelD A Scott, R Carmi, K Elbedour, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 17, 1999
Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR geneG A Fishman, E M Stone, S Grover, 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.
Experimental Eye Research|November 1, 1996
Preferential rod and cone photoreceptor abnormalities in heterozygotes with point mutations in the RDS geneS G Jacobson, A V Cideciyan, A M Maguire, 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.
Pageof 18