Artigo Acesso aberto Revisado por pares

Novel FGFR2 deletion in a patient with Beare–Stevenson‐like syndrome

2009; Wiley; Volume: 149A; Issue: 8 Linguagem: Inglês

10.1002/ajmg.a.32947

ISSN

1552-4833

Autores

Anne Slavotinek, Howard C. Crawford, Mahin Golabi, Cathy Tao, Hazel Perry, Sneha Oberoi, Karin Vargervik, Michael J. Friez,

Tópico(s)

Head and Neck Surgical Oncology

Resumo

American Journal of Medical Genetics Part AVolume 149A, Issue 8 p. 1814-1817 Research Letter Novel FGFR2 deletion in a patient with Beare–Stevenson-like syndrome† Anne Slavotinek, Corresponding Author Anne Slavotinek [email protected] Department of Pediatrics, University of California, San Francisco, San Francisco, CaliforniaDepartment of Pediatrics, University of California, San Francisco, Room U585P, 533 Parnassus St, San Francisco, CA 94143-0748.Search for more papers by this authorHoward Crawford, Howard Crawford Greenwood Genetics Center, One Gregor Mendel Circle, Greenwood, South CarolinaSearch for more papers by this authorMahin Golabi, Mahin Golabi Department of Pediatrics, University of California, San Francisco, San Francisco, CaliforniaSearch for more papers by this authorCathy Tao, Cathy Tao Division of Craniofacial Anomalies, Department of Orofacial Sciences, School of Dentistry, UCSF, San Francisco, CaliforniaSearch for more papers by this authorHazel Perry, Hazel Perry Division of Craniofacial Anomalies, Department of Orofacial Sciences, School of Dentistry, UCSF, San Francisco, CaliforniaSearch for more papers by this authorSneha Oberoi, Sneha Oberoi Division of Craniofacial Anomalies, Department of Orofacial Sciences, School of Dentistry, UCSF, San Francisco, CaliforniaSearch for more papers by this authorKarin Vargervik, Karin Vargervik Division of Craniofacial Anomalies, Department of Orofacial Sciences, School of Dentistry, UCSF, San Francisco, CaliforniaSearch for more papers by this authorMichael Friez, Michael Friez Greenwood Genetics Center, One Gregor Mendel Circle, Greenwood, South CarolinaSearch for more papers by this author Anne Slavotinek, Corresponding Author Anne Slavotinek [email protected] Department of Pediatrics, University of California, San Francisco, San Francisco, CaliforniaDepartment of Pediatrics, University of California, San Francisco, Room U585P, 533 Parnassus St, San Francisco, CA 94143-0748.Search for more papers by this authorHoward Crawford, Howard Crawford Greenwood Genetics Center, One Gregor Mendel Circle, Greenwood, South CarolinaSearch for more papers by this authorMahin Golabi, Mahin Golabi Department of Pediatrics, University of California, San Francisco, San Francisco, CaliforniaSearch for more papers by this authorCathy Tao, Cathy Tao Division of Craniofacial Anomalies, Department of Orofacial Sciences, School of Dentistry, UCSF, San Francisco, CaliforniaSearch for more papers by this authorHazel Perry, Hazel Perry Division of Craniofacial Anomalies, Department of Orofacial Sciences, School of Dentistry, UCSF, San Francisco, CaliforniaSearch for more papers by this authorSneha Oberoi, Sneha Oberoi Division of Craniofacial Anomalies, Department of Orofacial Sciences, School of Dentistry, UCSF, San Francisco, CaliforniaSearch for more papers by this authorKarin Vargervik, Karin Vargervik Division of Craniofacial Anomalies, Department of Orofacial Sciences, School of Dentistry, UCSF, San Francisco, CaliforniaSearch for more papers by this authorMichael Friez, Michael Friez Greenwood Genetics Center, One Gregor Mendel Circle, Greenwood, South CarolinaSearch for more papers by this author First published: 16 July 2009 https://doi.org/10.1002/ajmg.a.32947Citations: 15 † How to cite this article: Slavotinek A, Crawford H, Golabi M, Tao C, Perry H, Oberoi S, Vargervik K, Friez M. 2009. Novel FGFR2 deletion in a patient with Beare–Stevenson-like syndrome. Am J Med Genet Part A 149A:1814–1817. 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 Volume149A, Issue8August 2009Pages 1814-1817 RelatedInformation

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