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E M Stone

Showing results (121-130 of 174) with videos related to

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Human Molecular Genetics|August 1, 1994
Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mappingV C Sheffield, R Carmi, A Kwitek-Black, et al.
Human Molecular Genetics|May 1, 1997
Homozygosity mapping of achromatopsia to chromosome 2 using DNA poolingN C Arbour, J Zlotogora, R G Knowlton, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1991
Sister-chromatid separation and protein dephosphorylation in mitosisN Kinoshita, H Yamano, F Le Bouffant-Sladeczek, et al.
Ophthalmic Genetics|February 11, 1998
Clinical and molecular characterization of a family affected with X-linked ocular albinism (OA1)B L Lam, J H Fingert, B C Shutt, et al.
The British Journal of Ophthalmology|November 19, 2004
Genotype-phenotype correlation in a family with Arg135Leu rhodopsin retinitis pigmentosaK T Oh, D M Oh, R G Weleber, et al.
Journal of Glaucoma|December 12, 2001
Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patientsC Kawase, K Kawase, T Taniguchi, et al.
Ophthalmic Genetics|January 5, 2000
Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED lociA B Kanis, A A Al-Rajhi, C M Taylor, et al.
Nature Genetics|December 1, 1993
Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneityA E Kwitek-Black, R Carmi, G M Duyk, et al.
American Journal of Ophthalmology|December 22, 2000
A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathyJ B Kerrison, N R Miller, F Hsu, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 25, 2001
Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneityL A Donoso, A T Frost, E M Stone, et al.
Pageof 18

Showing results (121-130 of 174) with videos related to

Sort By:
Pageof 18
Human Molecular Genetics|August 1, 1994
Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mappingV C Sheffield, R Carmi, A Kwitek-Black, et al.
Human Molecular Genetics|May 1, 1997
Homozygosity mapping of achromatopsia to chromosome 2 using DNA poolingN C Arbour, J Zlotogora, R G Knowlton, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1991
Sister-chromatid separation and protein dephosphorylation in mitosisN Kinoshita, H Yamano, F Le Bouffant-Sladeczek, et al.
Ophthalmic Genetics|February 11, 1998
Clinical and molecular characterization of a family affected with X-linked ocular albinism (OA1)B L Lam, J H Fingert, B C Shutt, et al.
The British Journal of Ophthalmology|November 19, 2004
Genotype-phenotype correlation in a family with Arg135Leu rhodopsin retinitis pigmentosaK T Oh, D M Oh, R G Weleber, et al.
Journal of Glaucoma|December 12, 2001
Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patientsC Kawase, K Kawase, T Taniguchi, et al.
Ophthalmic Genetics|January 5, 2000
Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED lociA B Kanis, A A Al-Rajhi, C M Taylor, et al.
Nature Genetics|December 1, 1993
Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneityA E Kwitek-Black, R Carmi, G M Duyk, et al.
American Journal of Ophthalmology|December 22, 2000
A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathyJ B Kerrison, N R Miller, F Hsu, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|April 25, 2001
Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneityL A Donoso, A T Frost, E M Stone, et al.
Pageof 18