M M Sohocki - JoVE Visualize

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Molecular Vision|May 6, 1999

Identifying and mapping novel retinal-expressed ESTs from humansK Malone, M M Sohocki, L S Sullivan, et al.

Genomics|May 20, 1999

Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disordersM M Sohocki, K A Malone, L S Sullivan, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 23, 2001

Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humansM M Sohocki, L S Sullivan, D L Tirpak, et al.

Ophthalmic Genetics|August 1, 2000

Visual phenotype in patients with Arg41Gln and ala196+1bp mutations in the CRX geneR T Tzekov, M M Sohocki, S P Daiger, et al.

Investigative Ophthalmology & Visual Science|May 1, 2001

Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX geneR T Tzekov, Y Liu, M M Sohocki, et al.

Genomics|March 1, 1997

Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sitesM M Sohocki, L S Sullivan, W R Harrison, et al.

American Journal of Human Genetics|October 30, 1998

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor geneM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.

Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|September 8, 2001

Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17pK F Damji, M M Sohocki, R Khan, et al.

Ophthalmic Genetics|March 23, 2002

Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13)J J C van Lith-Verhoeven, S D van der Velde-Visser, M M Sohocki, et al.

Human Molecular Genetics|September 15, 1999

Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosaS J Bowne, S P Daiger, M M Hims, et al.

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Showing results (1-10 of 13) with videos related to

Sort By:

Pageof 2

Molecular Vision|May 6, 1999

Identifying and mapping novel retinal-expressed ESTs from humansK Malone, M M Sohocki, L S Sullivan, et al.

Genomics|May 20, 1999

Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disordersM M Sohocki, K A Malone, L S Sullivan, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 23, 2001

Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humansM M Sohocki, L S Sullivan, D L Tirpak, et al.

Ophthalmic Genetics|August 1, 2000

Visual phenotype in patients with Arg41Gln and ala196+1bp mutations in the CRX geneR T Tzekov, M M Sohocki, S P Daiger, et al.

Investigative Ophthalmology & Visual Science|May 1, 2001

Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX geneR T Tzekov, Y Liu, M M Sohocki, et al.

Genomics|March 1, 1997

Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sitesM M Sohocki, L S Sullivan, W R Harrison, et al.

American Journal of Human Genetics|October 30, 1998

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor geneM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.

Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|September 8, 2001

Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17pK F Damji, M M Sohocki, R Khan, et al.

Ophthalmic Genetics|March 23, 2002

Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13)J J C van Lith-Verhoeven, S D van der Velde-Visser, M M Sohocki, et al.

Human Molecular Genetics|September 15, 1999

Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosaS J Bowne, S P Daiger, M M Hims, et al.

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