Carpenter-Waziri syndrome results from a mutation in XNP
1999; Wiley; Volume: 85; Issue: 3 Linguagem: Inglês
10.1002/(sici)1096-8628(19990730)85
ISSN1096-8628
AutoresFatima Abidi, Charles E. Schwartz, Nancy J. Carpenter, Laurent Villard, Michel Font�s, Mary Curtis,
Tópico(s)Genomic variations and chromosomal abnormalities
ResumoAmerican Journal of Medical GeneticsVolume 85, Issue 3 p. 249-251 Letter to the Editor Carpenter-Waziri syndrome results from a mutation in XNP Fatima Abidi, Fatima Abidi Center for Molecular Studies, J.C. Self Research Institute, Greenwood Genetic Center, Greenwood, South CarolinaSearch for more papers by this authorCharles E. Schwartz, Corresponding Author Charles E. Schwartz schwartz@ggc.org Center for Molecular Studies, J.C. Self Research Institute, Greenwood Genetic Center, Greenwood, South CarolinaJ.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, 1 Gregor Mendel Circle, Greenwood, SC 29646Search for more papers by this authorNancy J. Carpenter, Nancy J. Carpenter H.A. Chapman Institute of Medical Genetics, Tulsa, OklahomaSearch for more papers by this authorLaurent Villard, Laurent Villard INSERM U491, Génétique Medicale et Développement, Faculté de Medicine, Marseille Cedex, FranceSearch for more papers by this authorMichel Fontés, Michel Fontés INSERM U491, Génétique Medicale et Développement, Faculté de Medicine, Marseille Cedex, FranceSearch for more papers by this authorMary Curtis, Mary Curtis University of Arkansas Medical School, Little Rock, ArkansasSearch for more papers by this author Fatima Abidi, Fatima Abidi Center for Molecular Studies, J.C. Self Research Institute, Greenwood Genetic Center, Greenwood, South CarolinaSearch for more papers by this authorCharles E. Schwartz, Corresponding Author Charles E. Schwartz schwartz@ggc.org Center for Molecular Studies, J.C. Self Research Institute, Greenwood Genetic Center, Greenwood, South CarolinaJ.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, 1 Gregor Mendel Circle, Greenwood, SC 29646Search for more papers by this authorNancy J. Carpenter, Nancy J. Carpenter H.A. Chapman Institute of Medical Genetics, Tulsa, OklahomaSearch for more papers by this authorLaurent Villard, Laurent Villard INSERM U491, Génétique Medicale et Développement, Faculté de Medicine, Marseille Cedex, FranceSearch for more papers by this authorMichel Fontés, Michel Fontés INSERM U491, Génétique Medicale et Développement, Faculté de Medicine, Marseille Cedex, FranceSearch for more papers by this authorMary Curtis, Mary Curtis University of Arkansas Medical School, Little Rock, ArkansasSearch for more papers by this author First published: 21 June 1999 https://doi.org/10.1002/(SICI)1096-8628(19990730)85:3 3.0.CO;2-UCitations: 38AboutPDF 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 No abstract is available for this article.Citing Literature Volume85, Issue3Special Issue: X-Linked Mental Retardation, Part III30 July 1999Pages 249-251 RelatedInformation
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