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• W2016455168 abstract "American Journal of Medical Genetics Part AVolume 161, Issue 4 p. 901-904 Research Letter 6p.24 microdeletion involving TFAP2A without classic features of branchio-oculo-facial syndrome† Shannon K. LeBlanc, Shannon K. LeBlanc Pediatric and Reproductive Genetics Unit, SA Pathology/Women's and Children's Hospital, South Australian Clinical Genetics Service, North Adelaide, South Australia, AustraliaSearch for more papers by this authorSui Yu, Sui Yu Genetics and Molecular Pathology, SA Pathology/Women's and Children's Hospital, North Adelaide, South Australia, AustraliaSearch for more papers by this authorChristopher P. Barnett, Corresponding Author Christopher P. Barnett [email protected] Pediatric and Reproductive Genetics Unit, SA Pathology/Women's and Children's Hospital, South Australian Clinical Genetics Service, North Adelaide, South Australia, AustraliaPediatric & Reproductive Genetics, Women's and Children's Hospital, SA Clinical Genetics Service, 72 King William Road, North Adelaide, SA 5006, Australia.Search for more papers by this author Shannon K. LeBlanc, Shannon K. LeBlanc Pediatric and Reproductive Genetics Unit, SA Pathology/Women's and Children's Hospital, South Australian Clinical Genetics Service, North Adelaide, South Australia, AustraliaSearch for more papers by this authorSui Yu, Sui Yu Genetics and Molecular Pathology, SA Pathology/Women's and Children's Hospital, North Adelaide, South Australia, AustraliaSearch for more papers by this authorChristopher P. Barnett, Corresponding Author Christopher P. Barnett [email protected] Pediatric and Reproductive Genetics Unit, SA Pathology/Women's and Children's Hospital, South Australian Clinical Genetics Service, North Adelaide, South Australia, AustraliaPediatric & Reproductive Genetics, Women's and Children's Hospital, SA Clinical Genetics Service, 72 King William Road, North Adelaide, SA 5006, Australia.Search for more papers by this author First published: 12 March 2013 https://doi.org/10.1002/ajmg.a.35804Citations: 5 † How to Cite this Article: LeBlanc SK, Yu S, Barnett CP. 2013. 6p.24 Microdeletion involving TFAP2A without classic features of branchio-oculo-facial syndrome. Am J Med Genet Part A 161A:901–904 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 Share a linkShare onFacebookTwitterLinkedInRedditWechat Citing Literature Volume161, Issue4April 2013Pages 901-904 RelatedInformation" @default.
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