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- W2038962637 abstract "Human MutationVolume 8, Issue 1 p. 85-88 Mutations in Brief Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndrome Sigrid Fuchs, Sigrid Fuchs Institut für Humangenetik, Universitäts-Krankenhaus Eppendorf, Butenfeld 32, D-22529 Hamburg, GermanySearch for more papers by this authorDorian van de Pol, Dorian van de Pol Department of Human Genetics, University Hospital, P.O. Box 9101, NL-6500 HB Nijmegen, the NetherlandsSearch for more papers by this authorUlrike Beudt, Ulrike Beudt Institut für Humangenetik, Universität Frankfurt, D-60696 Frankfurt, GermanySearch for more papers by this authorUlrich Kellner, Ulrich Kellner Universitätsklinikum Benjamin Franklin der FU Berlin, D-12200 Berlin, GermanySearch for more papers by this authorFrançoise Meire, Françoise Meire Department of Ophthalmology, University of Ghent, B-9000 Ghent, BelgiumSearch for more papers by this authorWolfgang Berger, Wolfgang Berger Department of Human Genetics, University Hospital, P.O. Box 9101, NL-6500 HB Nijmegen, the NetherlandsSearch for more papers by this authorAndreas Gal, Corresponding Author Andreas Gal Institut für Humangenetik, Universitäts-Krankenhaus Eppendorf, Butenfeld 32, D-22529 Hamburg, GermanyInstitut für Humangenetik, Universitäts-Krankenhaus Eppendorf, Butenfeld 32, D-22529 Hamburg, GermanySearch for more papers by this author Sigrid Fuchs, Sigrid Fuchs Institut für Humangenetik, Universitäts-Krankenhaus Eppendorf, Butenfeld 32, D-22529 Hamburg, GermanySearch for more papers by this authorDorian van de Pol, Dorian van de Pol Department of Human Genetics, University Hospital, P.O. Box 9101, NL-6500 HB Nijmegen, the NetherlandsSearch for more papers by this authorUlrike Beudt, Ulrike Beudt Institut für Humangenetik, Universität Frankfurt, D-60696 Frankfurt, GermanySearch for more papers by this authorUlrich Kellner, Ulrich Kellner Universitätsklinikum Benjamin Franklin der FU Berlin, D-12200 Berlin, GermanySearch for more papers by this authorFrançoise Meire, Françoise Meire Department of Ophthalmology, University of Ghent, B-9000 Ghent, BelgiumSearch for more papers by this authorWolfgang Berger, Wolfgang Berger Department of Human Genetics, University Hospital, P.O. Box 9101, NL-6500 HB Nijmegen, the NetherlandsSearch for more papers by this authorAndreas Gal, Corresponding Author Andreas Gal Institut für Humangenetik, Universitäts-Krankenhaus Eppendorf, Butenfeld 32, D-22529 Hamburg, GermanyInstitut für Humangenetik, Universitäts-Krankenhaus Eppendorf, Butenfeld 32, D-22529 Hamburg, GermanySearch for more papers by this author First published: 1996 https://doi.org/10.1002/(SICI)1098-1004(1996)8:1<85::AID-HUMU15>3.0.CO;2-NCitations: 7AboutPDF 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 Citing Literature Volume8, Issue11996Pages 85-88 RelatedInformation" @default.
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- W2038962637 title "Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndrome" @default.
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