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K W Small

Showing results (51-60 of 55) with videos related to

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Genomics|May 20, 1999
Bestrophin gene mutations in patients with Best vitelliform macular dystrophyG M Caldwell, L E Kakuk, I B Griesinger, et al.
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.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Genomics|May 20, 1999
Bestrophin gene mutations in patients with Best vitelliform macular dystrophyG M Caldwell, L E Kakuk, I B Griesinger, et al.
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.
Pageof 6