Author: "Gordon, A. H." / Database: Journals@OVID / Journal: human mutation - Searchworks@Jio Institute Digital Library Search Results

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Your search keyword '"Gordon, A. H."' showing total 3 results

Start Over Author "Gordon, A. H." Journal human mutation Database Journals@OVID

3 results on '"Gordon, A. H."'

1. A Rare Motor Neuron Deleterious Missense Mutation in the DPYSL3 (CRMP4) Gene is Associated with ALS

Author: Blasco, Hélène, Bernard-Marissal, Nathalie, Vourcʼh, Patrick, Guettard, Yves Olivier, Sunyach, Claire, Augereau, Olivier, Khederchah, Joelle, Mouzat, Kevin, Antar, Catherine, Gordon, Paul H., Veyrat-Durebex, Charlotte, Besson, Gérard, Andersen, Peter M., Salachas, François, Meininger, Vincent, Camu, William, Pettmann, Brigitte, Andres, Christian R., and Corcia, Philippe
Published: 2013
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2. High Frequency of Exon Deletions and Putative Founder Effects in French Canadian Lynch Syndrome Families

Author: Chong, George, Jarry, Jonathan, Marcus, Victoria, Thiffault, Isabelle, Winocour, Sebastian, Monczak, Yury, Drouin, Régen, Latreille, Jean, Australie, Karlene, Bapat, Bharati, Gordon, Philip H., Giguère, Yves, Gologan, Adrian, Galiatsatos, Polymnia, Jass, Jeremy R., Wong, Nora, Zaor, Sonya, Palma, Laura, Kasprzak, Lidia, Tischkowitz, Marc, and Foulkes, William D.
Published: 2009
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3. Distinct Patterns of Germ-Line Deletions in MLH1 and MSH2: The Implication of Alu Repetitive Element in the Genetic Etiology of Lynch Syndrome (HNPCC)

Author: Li, Lili, McVety, Susan, Younan, Rami, Liang, Ping, Sart, Desirée Du, Gordon, Philip H., Hutter, Pierre, Hogervorst, Frans B.L., Chong, George, and Foulkes, William D.
Published: 2006
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