R A Bush|P A Sieving - JoVE Visualize

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American Journal of Human Genetics|October 1, 1990

Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probesP A Sieving, E L Bingham, M S Roth, et al.

Investigative Ophthalmology & Visual Science|January 1, 1994

Dietary deficiency of N-3 fatty acids alters rhodopsin content and function in the rat retinaR A Bush, A Malnoë, C E Remé, et al.

Genomics|November 5, 1997

Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degenerationQ Farjo, A Jackson, S Pieke-Dahl, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|August 2, 2000

Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 geneL C Eksandh, V Ponjavic, R Ayyagari, et al.

Human Genetics|September 12, 2000

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacyR Ayyagari, L E Kakuk, E L Bingham, et al.

Military Medicine|March 29, 2001

Active surveillance of birth defects among U.S. Department of Defense beneficiaries: a feasibility studyR A Bush, T C Smith, W K Honner, et al.

Human Molecular Genetics|February 5, 1999

Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor functionA Swaroop, Q L Wang, W Wu, et al.

Nature Genetics|May 31, 2001

Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophyD A Thompson, Y Li, C L McHenry, et al.

Ophthalmic Genetics|July 23, 1999

A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutationR Mendoza-Londono, K T Hiriyanna, E L Bingham, et al.

American Journal of Human Genetics|October 27, 1997

Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, et al.

Pageof 10

Showing results (71-80 of 95) with videos related to

Sort By:

Pageof 10

American Journal of Human Genetics|October 1, 1990

Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probesP A Sieving, E L Bingham, M S Roth, et al.

Investigative Ophthalmology & Visual Science|January 1, 1994

Dietary deficiency of N-3 fatty acids alters rhodopsin content and function in the rat retinaR A Bush, A Malnoë, C E Remé, et al.

Genomics|November 5, 1997

Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degenerationQ Farjo, A Jackson, S Pieke-Dahl, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|August 2, 2000

Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 geneL C Eksandh, V Ponjavic, R Ayyagari, et al.

Human Genetics|September 12, 2000

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacyR Ayyagari, L E Kakuk, E L Bingham, et al.

Military Medicine|March 29, 2001

Active surveillance of birth defects among U.S. Department of Defense beneficiaries: a feasibility studyR A Bush, T C Smith, W K Honner, et al.

Human Molecular Genetics|February 5, 1999

Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor functionA Swaroop, Q L Wang, W Wu, et al.

Nature Genetics|May 31, 2001

Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophyD A Thompson, Y Li, C L McHenry, et al.

Ophthalmic Genetics|July 23, 1999

A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutationR Mendoza-Londono, K T Hiriyanna, E L Bingham, et al.

American Journal of Human Genetics|October 27, 1997

Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two familiesR Fujita, M Buraczynska, L Gieser, et al.

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