J A Klosterman|K W Small - JoVE Visualize

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Human Mutation|October 26, 1999

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence changeK T Hiriyanna, E L Bingham, B M Yashar, et al.

Nature Genetics|December 1, 1996

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeE V Semina, R Reiter, N J Leysens, et al.

Molecular Vision|January 5, 2000

North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysisK W Small, N Udar, S Yelchits, et al.

Human Molecular Genetics|July 27, 2001

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlationE De Baere, M J Dixon, K W Small, et al.

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Showing results (41-50 of 44) with videos related to

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You have reached the last page of results.This site can display upto 44 results.

Human Mutation|October 26, 1999

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence changeK T Hiriyanna, E L Bingham, B M Yashar, et al.

Nature Genetics|December 1, 1996

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeE V Semina, R Reiter, N J Leysens, et al.

Molecular Vision|January 5, 2000

North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysisK W Small, N Udar, S Yelchits, et al.

Human Molecular Genetics|July 27, 2001

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlationE De Baere, M J Dixon, K W Small, et al.

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