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Additional EFNB1 mutations in craniofrontonasal syndrome
2008; Wiley; Volume: 146A; Issue: 15 Linguagem: Inglês
10.1002/ajmg.a.32388
ISSN1552-4833
AutoresDeeann Wallis, Felicitas Lacbawan, Mahim Jain, Vazken M. Der Kaloustian, Carlos Eduardo Steiner, John B. Moeschler, H. Wolfgang Losken, Ilkka Kaitila, Stephen Cantrell, Virginia K. Proud, John C. Carey, Donald W. Day, Dorit Lev, Ahmad S. Teebi, Luther K. Robinson, H. Eugene Hoyme, N.A. Al‐Torki, Jacqueline Siegel‐Bartelt, John B. Mulliken, Nathaniel H. Robin, Dolores Saavedra, Elaine H. Zackai, Maximilian Muenke,
Tópico(s)Connective tissue disorders research
ResumoAmerican Journal of Medical Genetics Part AVolume 146A, Issue 15 p. 2008-2012 Research Letter Additional EFNB1 mutations in craniofrontonasal syndrome†‡ Deeann Wallis, Deeann Wallis Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MarylandSearch for more papers by this authorFelicitas Lacbawan, Felicitas Lacbawan Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MarylandSearch for more papers by this authorMahim Jain, Mahim Jain Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MarylandSearch for more papers by this authorVazken M. Der Kaloustian, Vazken M. Der Kaloustian McGill University Health Center, Montreal, CanadaSearch for more papers by this authorCarlos E. Steiner, Carlos E. Steiner Department of Medical Genetics, Unicamp, Campinas, Sao Paulo, BrazilSearch for more papers by this authorJohn B. Moeschler, John B. Moeschler Dartmouth Medical Center, Lebanon, New HampshireSearch for more papers by this authorH. Wolfgang Losken, H. Wolfgang Losken University of Pittsburgh, Pittsburgh, PennsylvaniaSearch for more papers by this authorIlkka I. Kaitila, Ilkka I. Kaitila Haartman Institute, University of Helsinki, Helsinki, FinlandSearch for more papers by this authorStephen Cantrell, Stephen Cantrell New Jersey Dental School, Newark, New JerseySearch for more papers by this authorVirginia K. Proud, Virginia K. Proud Children's Hospital of the King's Daughters, Norfolk, VirginiaSearch for more papers by this authorJohn C. Carey, John C. Carey University of Utah Medical Center, Salt Lake City, UtahSearch for more papers by this authorDonald W. Day, Donald W. Day Private Practice, Hewitt, TexasSearch for more papers by this authorDorit Lev, Dorit Lev Institute of Clinical Genetics, Wolfson Medical Genetics Center, Holon, IsraelSearch for more papers by this authorAhmad S. Teebi, Ahmad S. Teebi Weill Cornell Medical College, New York, New YorkSearch for more papers by this authorLuther K. Robinson, Luther K. Robinson Buffalo School of Medicine and Biomedical Sciences, Buffalo, New YorkSearch for more papers by this authorH. Eugene Hoyme, H. Eugene Hoyme Stanford University School of Medicine, Stanford, CaliforniaSearch for more papers by this authorNadia Al-Torki, Nadia Al-Torki Kuwait Medical Genetics Center, Sulibihkhat, KuwaitSearch for more papers by this authorJacqueline Siegel-Bartelt, Jacqueline Siegel-Bartelt The Genetics Institute, Pasadena, CaliforniaSearch for more papers by this authorJohn B. Mulliken, John B. Mulliken Children's Hospital Boston, Harvard Medical School, Boston, MassachusettsSearch for more papers by this authorNathaniel H. Robin, Nathaniel H. Robin University of Alabama, Birmingham, AlabamaSearch for more papers by this authorDolores Saavedra, Dolores Saavedra Hospital General Dr. Manuel Gea Gonzáles, Mexico City, MexicoSearch for more papers by this authorElaine H. Zackai, Elaine H. Zackai Division of Human and Molecular Genetics, The Children's Hospital of Philadelphia, Philadelphia, PennsylvaniaSearch for more papers by this authorMaximilian Muenke, Corresponding Author Maximilian Muenke [email protected] Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MarylandMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, 35 Convent Drive-MSC 3717, Building 35, Room 1B-203, Bethesda, MD 20892-3717.Search for more papers by this author Deeann Wallis, Deeann Wallis Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MarylandSearch for more papers by this authorFelicitas Lacbawan, Felicitas Lacbawan Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MarylandSearch for more papers by this authorMahim Jain, Mahim Jain Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MarylandSearch for more papers by this authorVazken M. Der Kaloustian, Vazken M. Der Kaloustian McGill University Health Center, Montreal, CanadaSearch for more papers by this authorCarlos E. Steiner, Carlos E. Steiner Department of Medical Genetics, Unicamp, Campinas, Sao Paulo, BrazilSearch for more papers by this authorJohn B. Moeschler, John B. Moeschler Dartmouth Medical Center, Lebanon, New HampshireSearch for more papers by this authorH. Wolfgang Losken, H. Wolfgang Losken University of Pittsburgh, Pittsburgh, PennsylvaniaSearch for more papers by this authorIlkka I. Kaitila, Ilkka I. Kaitila Haartman Institute, University of Helsinki, Helsinki, FinlandSearch for more papers by this authorStephen Cantrell, Stephen Cantrell New Jersey Dental School, Newark, New JerseySearch for more papers by this authorVirginia K. Proud, Virginia K. Proud Children's Hospital of the King's Daughters, Norfolk, VirginiaSearch for more papers by this authorJohn C. Carey, John C. Carey University of Utah Medical Center, Salt Lake City, UtahSearch for more papers by this authorDonald W. Day, Donald W. Day Private Practice, Hewitt, TexasSearch for more papers by this authorDorit Lev, Dorit Lev Institute of Clinical Genetics, Wolfson Medical Genetics Center, Holon, IsraelSearch for more papers by this authorAhmad S. Teebi, Ahmad S. Teebi Weill Cornell Medical College, New York, New YorkSearch for more papers by this authorLuther K. Robinson, Luther K. Robinson Buffalo School of Medicine and Biomedical Sciences, Buffalo, New YorkSearch for more papers by this authorH. Eugene Hoyme, H. Eugene Hoyme Stanford University School of Medicine, Stanford, CaliforniaSearch for more papers by this authorNadia Al-Torki, Nadia Al-Torki Kuwait Medical Genetics Center, Sulibihkhat, KuwaitSearch for more papers by this authorJacqueline Siegel-Bartelt, Jacqueline Siegel-Bartelt The Genetics Institute, Pasadena, CaliforniaSearch for more papers by this authorJohn B. Mulliken, John B. Mulliken Children's Hospital Boston, Harvard Medical School, Boston, MassachusettsSearch for more papers by this authorNathaniel H. Robin, Nathaniel H. Robin University of Alabama, Birmingham, AlabamaSearch for more papers by this authorDolores Saavedra, Dolores Saavedra Hospital General Dr. Manuel Gea Gonzáles, Mexico City, MexicoSearch for more papers by this authorElaine H. Zackai, Elaine H. Zackai Division of Human and Molecular Genetics, The Children's Hospital of Philadelphia, Philadelphia, PennsylvaniaSearch for more papers by this authorMaximilian Muenke, Corresponding Author Maximilian Muenke [email protected] Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MarylandMedical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, 35 Convent Drive-MSC 3717, Building 35, Room 1B-203, Bethesda, MD 20892-3717.Search for more papers by this author First published: 14 July 2008 https://doi.org/10.1002/ajmg.a.32388Citations: 21 † This article is a US Government work and, as such, is in the public domain in the United States of America. ‡ How to cite this article: Wallis D, Lacbawan F, Jain M, Der Kaloustian VM, Steiner CE, Moeschler JB, Losken HW, Kaitila II, Cantrell S, Proud VK, Carey JC, Day DW, Lev D, Teebi AS, Robinson LK, Hoyme HE, Al-Torki N, Siegel-Bartelt J, Mulliken JB, Robin NH, Saavedra D, Zackai EH, Muenke M. 2008. Additional EFNB1 mutations in craniofrontonasal syndrome. Am J Med Genet Part A 146A:2008–2012. 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 Citing Literature Volume146A, Issue151 August 2008Pages 2008-2012 RelatedInformation
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