DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature

Abstract

American Journal of Medical GeneticsVolume 83, Issue 4 p. 347-349 Letter to the Editor DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature Pietro Chiurazzi, Corresponding Author Pietro Chiurazzi ibige@rm.unicatt.it Istituto di Genetica Medica, Università Cattolica and Centro Ricerche per la Disabilità Mentale e Motoria, Associazione “Anni Verdi”, Rome, ItalyIstituto di Genetica Medica, Università Cattolica, L. go F. Vito 1, 00168 Roma, ItalySearch for more papers by this authorM. Grazia Pomponi, M. Grazia Pomponi Istituto di Genetica Medica, Università Cattolica and Centro Ricerche per la Disabilità Mentale e Motoria, Associazione “Anni Verdi”, Rome, ItalySearch for more papers by this authorAndrea Sharrock, Andrea Sharrock Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, United KingdomSearch for more papers by this authorJames Macpherson, James Macpherson Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, United KingdomSearch for more papers by this authorSébastien Lormeau, Sébastien Lormeau Réseau de Médecine Génétique Appliquée—FRSQ, Centre de Recherche en Droit Public, Université de Montréal, Montreal, CanadaSearch for more papers by this authorMarie Lou Morel, Marie Lou Morel Unité de Recherche en Genetique Humaine et Moleculaire, Centre Hospitalier Universitaire de Québec-PSFA, Université Laval, Quebec, CanadaSearch for more papers by this authorFrançois Rousseau, François Rousseau Unité de Recherche en Genetique Humaine et Moleculaire, Centre Hospitalier Universitaire de Québec-PSFA, Université Laval, Quebec, CanadaSearch for more papers by this author Pietro Chiurazzi, Corresponding Author Pietro Chiurazzi ibige@rm.unicatt.it Istituto di Genetica Medica, Università Cattolica and Centro Ricerche per la Disabilità Mentale e Motoria, Associazione “Anni Verdi”, Rome, ItalyIstituto di Genetica Medica, Università Cattolica, L. go F. Vito 1, 00168 Roma, ItalySearch for more papers by this authorM. Grazia Pomponi, M. Grazia Pomponi Istituto di Genetica Medica, Università Cattolica and Centro Ricerche per la Disabilità Mentale e Motoria, Associazione “Anni Verdi”, Rome, ItalySearch for more papers by this authorAndrea Sharrock, Andrea Sharrock Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, United KingdomSearch for more papers by this authorJames Macpherson, James Macpherson Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, United KingdomSearch for more papers by this authorSébastien Lormeau, Sébastien Lormeau Réseau de Médecine Génétique Appliquée—FRSQ, Centre de Recherche en Droit Public, Université de Montréal, Montreal, CanadaSearch for more papers by this authorMarie Lou Morel, Marie Lou Morel Unité de Recherche en Genetique Humaine et Moleculaire, Centre Hospitalier Universitaire de Québec-PSFA, Université Laval, Quebec, CanadaSearch for more papers by this authorFrançois Rousseau, François Rousseau Unité de Recherche en Genetique Humaine et Moleculaire, Centre Hospitalier Universitaire de Québec-PSFA, Université Laval, Quebec, CanadaSearch for more papers by this author First published: 24 March 1999 https://doi.org/10.1002/(SICI)1096-8628(19990402)83:4<347::AID-AJMG25>3.0.CO;2-%23Citations: 14AboutPDF 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 onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume83, Issue4Special Issue: X-Linked Mental Retardation, Part I2 April 1999Pages 347-349 RelatedInformation