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- W2058201722 abstract "Clinical GeneticsVolume 76, Issue 3 p. 296-299 Characterization of a novel FOXC1 mutation, P297S, identified in two individuals with anterior segment dysgenesis CD Fetterman, CD Fetterman Department of Medical Genetics, University of Alberta, Edmonton, Alberta, CanadaSearch for more papers by this authorF Mirzayans, F Mirzayans Department of Medical Genetics, University of Alberta, Edmonton, Alberta, CanadaSearch for more papers by this authorMA Walter, MA Walter Department of Medical Genetics, University of Alberta, Edmonton, Alberta, CanadaSearch for more papers by this author CD Fetterman, CD Fetterman Department of Medical Genetics, University of Alberta, Edmonton, Alberta, CanadaSearch for more papers by this authorF Mirzayans, F Mirzayans Department of Medical Genetics, University of Alberta, Edmonton, Alberta, CanadaSearch for more papers by this authorMA Walter, MA Walter Department of Medical Genetics, University of Alberta, Edmonton, Alberta, CanadaSearch for more papers by this author First published: 24 September 2009 https://doi.org/10.1111/j.1399-0004.2009.01210.xCitations: 8 Michael A. WalterDepartment of Medical GeneticsUniversity of Alberta839 Medical Sciences BuildingEdmontonAlbertaCanada T6G 2H7.Tel.: +780 492 9044;fax: +780 492 1998e-mail: mwalter@ualberta.ca Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume76, Issue3September 2009Pages 296-299 RelatedInformation" @default.
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- W2058201722 title "Characterization of a novel FOXC1 mutation, P297S, identified in two individuals with anterior segment dysgenesis" @default.
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