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M J Denton

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Human Genetics|January 1, 1991
No evidence of linkage between the locus for autosomal dominant retinitis pigmentosa and D3S47 (C17) in three Australian familiesJ B Jiménez, C Samanns, A Watty, et al.
Clinical Genetics|March 1, 1995
Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from PakistanJ Leutelt, R Oehlmann, F Younus, et al.
Ophthalmic Genetics|September 18, 2001
CRB1 mutations may result in retinitis pigmentosa without para-arteriolar RPE preservationA J Lotery, A Malik, S A Shami, et al.
Genomics|April 18, 1998
Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3U Finckh, S Xu, G Kumaramanickavel, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990
Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity testsJ Ott, S Bhattacharya, J D Chen, et al.
Nature Genetics|November 5, 1997
Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosaM A Maw, B Kennedy, A Knight, et al.
Nature Genetics|November 5, 1997
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophyS M Gu, D A Thompson, C R Srikumari, et al.
Genomics|April 1, 1988
Two different genes for X-linked retinitis pigmentosaB Wirth, M J Denton, J D Chen, et al.
Human Molecular Genetics|December 10, 1999
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degenerationM A Maw, D Corbeil, J Koch, et al.
Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Human Genetics|January 1, 1991
No evidence of linkage between the locus for autosomal dominant retinitis pigmentosa and D3S47 (C17) in three Australian familiesJ B Jiménez, C Samanns, A Watty, et al.
Clinical Genetics|March 1, 1995
Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from PakistanJ Leutelt, R Oehlmann, F Younus, et al.
Ophthalmic Genetics|September 18, 2001
CRB1 mutations may result in retinitis pigmentosa without para-arteriolar RPE preservationA J Lotery, A Malik, S A Shami, et al.
Genomics|April 18, 1998
Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3U Finckh, S Xu, G Kumaramanickavel, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990
Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity testsJ Ott, S Bhattacharya, J D Chen, et al.
Nature Genetics|November 5, 1997
Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosaM A Maw, B Kennedy, A Knight, et al.
Nature Genetics|November 5, 1997
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophyS M Gu, D A Thompson, C R Srikumari, et al.
Genomics|April 1, 1988
Two different genes for X-linked retinitis pigmentosaB Wirth, M J Denton, J D Chen, et al.
Human Molecular Genetics|December 10, 1999
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degenerationM A Maw, D Corbeil, J Koch, et al.
Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.
Pageof 5