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B R Powell

Showing results (21-30 of 26) with videos related to

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Clinical Chemistry|February 1, 1990
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency as detected by radiochemical assay in cell extracts by thin-layer chromatography, and identification of three new casesK M Gibson, C F Lee, V Kamali, et al.
Nature Genetics|May 1, 1993
Dystrophin expression in the human retina is required for normal function as defined by electroretinographyD A Pillers, D E Bulman, R G Weleber, et al.
Ophthalmology|May 1, 1994
Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophyD A Sigesmund, R G Weleber, D A Pillers, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndromeD A Pillers, W K Seltzer, B R Powell, et al.
Human Genetics|September 10, 1999
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutationsD A Pillers, K M Fitzgerald, N M Duncan, et al.
Human Molecular Genetics|April 4, 2001
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)D Y Nishimura, C C Searby, R Carmi, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Clinical Chemistry|February 1, 1990
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency as detected by radiochemical assay in cell extracts by thin-layer chromatography, and identification of three new casesK M Gibson, C F Lee, V Kamali, et al.
Nature Genetics|May 1, 1993
Dystrophin expression in the human retina is required for normal function as defined by electroretinographyD A Pillers, D E Bulman, R G Weleber, et al.
Ophthalmology|May 1, 1994
Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophyD A Sigesmund, R G Weleber, D A Pillers, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndromeD A Pillers, W K Seltzer, B R Powell, et al.
Human Genetics|September 10, 1999
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutationsD A Pillers, K M Fitzgerald, N M Duncan, et al.
Human Molecular Genetics|April 4, 2001
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)D Y Nishimura, C C Searby, R Carmi, et al.
Pageof 3