Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13) von MCKIE, Arthur B, MCHALE, John C, MACKEY, David A, BHATTACHARYA, Shomi S, BIRD, Alan C, MARKHAM, Alexander F, INGLEHEARN, Chris F, KEEN, T. Jeffrey, TARTTELIN, Emma E, GOLIATH, Rene, VAN LITH-VERHOEVEN, Janneke J. C, GREENBERG, Jacquie, RAMESAR, Rajkumar S, HOYNG, Carel B, CREMERS, Frans P. M

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PAP-1, the mutated gene underlying the RP9 form of dominant retinitis pigmentosa, is a splicing factor von Maita, Hiroshi, Kitaura, Hirotake, Keen, T. Jeffrey, Inglehearn, Chris F., Ariga, Hiroyoshi, Iguchi-Ariga, Sanae M.M.

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Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36 von Keen, T Jeffrey, Mohamed, Moin D, McKibbin, Martin, Rashid, Yasmin, Jafri, Hussain, Maumenee, Irene H, Inglehearn, Chris F

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Differential expression of particulate methane monooxygenase genes in the verrucomicrobial methanotroph ‘Methylacidiphilum kamchatkense’ Kam1 von Erikstad, Helge-André, Jensen, Sigmund, Keen, T. Jeffrey, Birkeland, Nils-Kåre

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Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa von CHAKAROVA, Christina F, HIMS, Matthew M, ROSENBERG, Thomas, WEBSTER, Andrew R, BIRD, Alan C, GAL, Andreas, HUNT, David, VITHANA, Eranga N, BHATTACHARYA, Shomi S, BOLZ, Hanno, ABU-SAFIEH, Leen, PATEL, Reshma J, PAPAIOANNOU, Myrto G, INGLEHEARN, Chris F, KEEN, T. Jeffrey, WILLIS, Catherine, MOORE, Anthony T

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Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa von Keen, T Jeffrey, Hims, Matthew M, McKie, Arthur B, Moore, Anthony T, Doran, Rob M, Mackey, David A, Mansfield, David C, Mueller, Robert F, Bhattacharya, Shomi S, Bird, Alan C, Markham, Alexander F, Inglehearn, Chris F

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Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate von Downey, Louise M, Keen, T Jeffrey, Jalili, Ismail K, McHale, John, Aldred, Michael J, Robertson, Steven P, Mighell, Alan, Fayle, Steven, Wissinger, Bernd, Inglehearn, Chris F

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Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19 von Al-Maghtheh, Mai, Inglehearn, Chris F., Jeffrey, T. Keen, Evans, Kevin, Moore, Anthony T., Jay, Marcelle, Bird, Alan C., Bhattacharya, Shomi S.

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Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation von Moore, A T, Fitzke, F W, Kemp, C M, Arden, G B, Keen, T J, Inglehearn, C F, Bhattacharya, S S, Bird, A C

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Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa

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Mutations and polymorphisms in the human peripherin-RDS gene and their involvement in inherited retinal degeneration von Keen, T. Jeffrey, Inglehearn, Chris F.

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A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis piamentosa von Inglehearn, Chris F., Keen, T. Jeffrey, Bashir, Rumaisa, Jay, Marcelle, Fitzke, Fred, C.Bird, Alan, Crombie, Alex, Bhattacharya, Shomi

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Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin geneother von Keen, T.Jeffrey, Ingleheam, Chris F., Kim, Robert, Bird, Alan C., Bhattacharya, Shoml

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Macular Dystrophy Associated with Mutations at Codon 172 in the Human Retinal Degeneration Slow Gene von Wroblewski, John J., Wells, John A., Eckstein, Anja, Fitzke, Fred, Jubb, Chris, Keen, T. Jeffrey, Inglehearn, Chris, Bhattacharya, Shomi, Arden, Geoffrey B., Jay, Marcelle, Bird, Alan C.

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Analysis of a Human Gene Homologous to Rat Ventral Prostate.1 Protein von Peacock, Rachel E., Keen, T.Jeffrey, Inglehearn, Chris F.

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Mutations in HPRP3, a third member ofpre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa von Chakarova, C. F.

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Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities von Reynolds, Paul A., Powlesland, Rachel M., Keen, T. Jeffrey, Inglehearn, Chris F., Cunningham, Aimee F., Green, Eric D., Brown, Keith W.

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Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa families von Keen, T J, Morris, A G, Inglehearn, C F

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The Practice of Pre-Therapy von Prouty, Garry F

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A YAC Contig Spanning the Dominant Retinitis Pigmentosa Locus (RP9) on Chromosome 7p von Keen, T.Jeffrey, Inglehearn, Chris F., Green, Eric D., Cunningham, Aimee F., Patel, Reshma J., Peacock, Rachel E., Gerken, Steve, White, Ray, Weissenbach, Jean, Bhattacharya, Shomi S.

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