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Results: 1-4 |
Results: 4

Authors: O'Reilly, Mary Palfi, Arpad Chadderton, Naomi Millington-Ward, Sophia Ader, Marius Cronin, Thérèse Tuohy, Thérèse Auricchio, Alberto Hildinger, Markus Tivnan, Amanda McNally, Niamh Humphries, Marian M. Kiang, Anna-Sophia Humphries, Pete Kenna, Paul F. Farrar, G. Jane
Citation: O'Reilly, Mary et al., RNA Interference.Mediated Suppression and Replacement of Human Rhodopsin In Vivo, American journal of human genetics , 81(1), 2007, pp. 127-135

Authors: Bradley, Daniel G. Farrar, G. Jane Sharp, Elizabeth M. Kenna, Paul Humphries, Marian M. McConnell, David J. Daiger, Stephen P. McWilliam, Peter Humphries, Peter
Citation: G. Bradley, Daniel et al., Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome i including the region surrounding the rhesus locus, American journal of human genetics , 44(4), 1989, pp. 570-576

Authors: Inglehearn, Chris F. Lester, Douglas H. Bashir, Rumaisa Atif, Uzma Keen, T. Jeffrey Sertedaki, Amalia Lindsey, Janet Jay, Marcelle Bird, Alan C. Farrar, G. Jane Humphries, Peter Bhattacharya, Shomi S.
Citation: F. Inglehearn, Chris et al., Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa families, American journal of human genetics , 50-I(3), 1992, pp. 590-597

Authors: Jordan, SiobhAn A. Farrar, G. Jane Kumar-Singh, Rajendra Kenna, Paul Humphries, Marian M. Allamand, Valérie Sharp, Elizabeth M. Humphries, Peter
Citation: A. Jordan, Siobhan et al., Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin., American journal of human genetics , 50-I(3), 1992, pp. 634-639
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