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E M Stone

Showing results (51-60 of 174) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|November 21, 1997
X-linked retinitis pigmentosa associated with a 2-base pair insertion in codon 99 of the RP3 gene RPGRR G Weleber, N S Butler, W H Murphey, et al.
Nature|January 9, 1998
Connexin mutations and hearing lossD A Scott, M L Kraft, E M Stone, et al.
Journal of the American Academy of Dermatology|August 1, 1993
Incontinentia pigmenti: transmission from father to daughterM M Emery, E C Siegfried, M S Stone, 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.
Investigative Ophthalmology & Visual Science|July 1, 1996
Photoreceptor function in heterozygotes with insertion or deletion mutations in the RDS geneS G Jacobson, A V Cideciyan, C M Kemp, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/RDS geneR G Weleber, R E Carr, W H Murphey, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 26, 1998
DNA adducts in human breast tissue: association with N-acetyltransferase-2 (NAT2) and NAT1 genotypesW Pfau, E M Stone, U Brockstedt, et al.
Retina (Philadelphia, Pa.)|January 5, 2002
Visual outcome following subretinal hemorrhage in Best diseaseM M Chung, K T Oh, L M Streb, et al.
Carcinogenesis|July 11, 1998
Interindividual variation in the metabolic activation of heterocyclic amines and their N-hydroxy derivatives in primary cultures of human mammary epithelial cellsE M Stone, J A Williams, P L Grover, et al.
Journal of Clinical Neuro-Ophthalmology|December 1, 1990
Optic nerve sheath distention in Leber's optic neuropathy and the significance of the "Wallace mutation"J L Smith, D T Tse, S F Byrne, et al.
Pageof 18

Showing results (51-60 of 174) with videos related to

Sort By:
Pageof 18
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 21, 1997
X-linked retinitis pigmentosa associated with a 2-base pair insertion in codon 99 of the RP3 gene RPGRR G Weleber, N S Butler, W H Murphey, et al.
Nature|January 9, 1998
Connexin mutations and hearing lossD A Scott, M L Kraft, E M Stone, et al.
Journal of the American Academy of Dermatology|August 1, 1993
Incontinentia pigmenti: transmission from father to daughterM M Emery, E C Siegfried, M S Stone, 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.
Investigative Ophthalmology & Visual Science|July 1, 1996
Photoreceptor function in heterozygotes with insertion or deletion mutations in the RDS geneS G Jacobson, A V Cideciyan, C M Kemp, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/RDS geneR G Weleber, R E Carr, W H Murphey, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 26, 1998
DNA adducts in human breast tissue: association with N-acetyltransferase-2 (NAT2) and NAT1 genotypesW Pfau, E M Stone, U Brockstedt, et al.
Retina (Philadelphia, Pa.)|January 5, 2002
Visual outcome following subretinal hemorrhage in Best diseaseM M Chung, K T Oh, L M Streb, et al.
Carcinogenesis|July 11, 1998
Interindividual variation in the metabolic activation of heterocyclic amines and their N-hydroxy derivatives in primary cultures of human mammary epithelial cellsE M Stone, J A Williams, P L Grover, et al.
Journal of Clinical Neuro-Ophthalmology|December 1, 1990
Optic nerve sheath distention in Leber's optic neuropathy and the significance of the "Wallace mutation"J L Smith, D T Tse, S F Byrne, et al.
Pageof 18