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D A Mackey

Showing results (61-70 of 65) with videos related to

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Human Molecular Genetics|July 7, 2001
Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophyC Toomes, N J Marchbank, D A Mackey, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Science (New York, N.Y.)|January 31, 1997
Identification of a gene that causes primary open angle glaucomaE M Stone, J H Fingert, W L Alward, et al.
Human Molecular Genetics|July 27, 2001
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)A B McKie, J C McHale, T J Keen, et al.
Human Molecular Genetics|April 10, 1999
Analysis of myocilin mutations in 1703 glaucoma patients from five different populationsJ H Fingert, E Héon, J M Liebmann, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Human Molecular Genetics|July 7, 2001
Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophyC Toomes, N J Marchbank, D A Mackey, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Science (New York, N.Y.)|January 31, 1997
Identification of a gene that causes primary open angle glaucomaE M Stone, J H Fingert, W L Alward, et al.
Human Molecular Genetics|July 27, 2001
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)A B McKie, J C McHale, T J Keen, et al.
Human Molecular Genetics|April 10, 1999
Analysis of myocilin mutations in 1703 glaucoma patients from five different populationsJ H Fingert, E Héon, J M Liebmann, et al.
Pageof 7