| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 15980210 [Unique ID], provided by the PubMed system | |
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| Riazuddin SA, Zulfiqar F, Zhang Q, et al.
Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families. [Journal Article]
Invest Ophthalmol Vis Sci 2005 Jul; 46(7):2264-70.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Zhang Q, Zulfiqar F, Riazuddin SA, et al.
Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation. [Journal Article]
Mol Vis 2004 Nov 17.:884-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Riazuddin SA, Zulfiqar F, Zhang Q, et al.
Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani families. [Journal Article, Research Support, N.I.H., Intramural, Research Support, Non-U.S. Gov't]
Mol Vis 2006.:1283-91.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Riazuddin SA, Yasmeen A, Yao W, et al.
Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families. [Journal Article]
Invest Ophthalmol Vis Sci 2005 Jun; 46(6):2100-6.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Hameed A, Khaliq S, Ismail M, et al.
A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family. [Journal Article]
Invest Ophthalmol Vis Sci 2001 Jun; 42(7):1436-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Payne A, Vithana E, Khaliq S, et al.
RP1 protein truncating mutations predominate at the RP1 adRP locus. [Journal Article]
Invest Ophthalmol Vis Sci 2000 Dec; 41(13):4069-73.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Bowne SJ, Daiger SP, Hims MM, et al.
Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa. [Journal Article]
Hum Mol Genet 1999 Oct; 8(11):2121-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | den Hollander AI, van Lith-Verhoeven JJ, Arends ML, et al.
Novel compound heterozygous TULP1 mutations in a family with severe early-onset retinitis pigmentosa. [Journal Article, Research Support, Non-U.S. Gov't]
Arch Ophthalmol 2007 Jul; 125(7):932-5.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Baum L, Chan WM, Yeung KY, et al.
RP1 in Chinese: Eight novel variants and evidence that truncation of the extreme C-terminal does not cause retinitis pigmentosa. [Journal Article]
Hum Mutat 2001 May; 17(5):436.
Abstract | Full Citation | Publisher Full Text | Find Related Articles |   |
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