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D Stambolian

Showing results (11-20 of 29) with videos related to

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Genomics|July 15, 1994
Mapping of the X-linked cataract (Xcat) mutation, the gene implicated in the Nance Horan syndrome, on the mouse X chromosomeD Stambolian, J Favor, W Silvers, et al.
Investigative Ophthalmology & Visual Science|March 1, 1986
Cataracts in patients heterozygous for galactokinase deficiencyD Stambolian, V Scarpino-Myers, R C Eagle, et al.
Investigative Ophthalmology & Visual Science|September 4, 1998
Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8P A Grimes, B Koeberlein, J Favor, et al.
Molecular Biology and Evolution|May 1, 1990
Ribosomal RNA gene sequences and hominoid phylogenyI L Gonzalez, J E Sylvester, T F Smith, et al.
American Journal of Ophthalmology|November 13, 2001
Lens changes in hereditary hyperferritinemia-cataract syndromeA Chang-Godinich, S Ades, D Schenkein, et al.
Experimental Eye Research|November 1, 1993
Lens development in a dominant X-linked congenital cataract of the mouseP A Grimes, J Favor, B Koeberlein, et al.
Nature Genetics|July 1, 1995
Cloning of the galactokinase cDNA and identification of mutations in two families with cataractsD Stambolian, Y Ai, D Sidjanin, et al.
Metabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)|January 1, 1985
Macular deposits in galactokinase deficiencyB L Hodes, J M Schietroma, S S Lane, et al.
Journal of Molecular Biology|March 5, 1990
Sequence and structure correlation of human ribosomal transcribed spacersI L Gonzalez, C Chambers, J L Gorski, et al.
Genome Research|August 1, 1995
Mouse galactokinase: isolation, characterization, and location on chromosome 11Y Ai, N A Jenkins, N G Copeland, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Genomics|July 15, 1994
Mapping of the X-linked cataract (Xcat) mutation, the gene implicated in the Nance Horan syndrome, on the mouse X chromosomeD Stambolian, J Favor, W Silvers, et al.
Investigative Ophthalmology & Visual Science|March 1, 1986
Cataracts in patients heterozygous for galactokinase deficiencyD Stambolian, V Scarpino-Myers, R C Eagle, et al.
Investigative Ophthalmology & Visual Science|September 4, 1998
Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8P A Grimes, B Koeberlein, J Favor, et al.
Molecular Biology and Evolution|May 1, 1990
Ribosomal RNA gene sequences and hominoid phylogenyI L Gonzalez, J E Sylvester, T F Smith, et al.
American Journal of Ophthalmology|November 13, 2001
Lens changes in hereditary hyperferritinemia-cataract syndromeA Chang-Godinich, S Ades, D Schenkein, et al.
Experimental Eye Research|November 1, 1993
Lens development in a dominant X-linked congenital cataract of the mouseP A Grimes, J Favor, B Koeberlein, et al.
Nature Genetics|July 1, 1995
Cloning of the galactokinase cDNA and identification of mutations in two families with cataractsD Stambolian, Y Ai, D Sidjanin, et al.
Metabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)|January 1, 1985
Macular deposits in galactokinase deficiencyB L Hodes, J M Schietroma, S S Lane, et al.
Journal of Molecular Biology|March 5, 1990
Sequence and structure correlation of human ribosomal transcribed spacersI L Gonzalez, C Chambers, J L Gorski, et al.
Genome Research|August 1, 1995
Mouse galactokinase: isolation, characterization, and location on chromosome 11Y Ai, N A Jenkins, N G Copeland, et al.
Pageof 3