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Material Type: Artigo
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Phenotypic and mutational spectrum of ROR2-related Robinow syndromeAriadne R. Lima Barbara M Ferreira; Chaofan Zhang; Angad Jolly; Haowei Du; Janson J White; Moez Dawood; Tulio C Lins; Marcela A Chiabai; Ellen van Beusekom; Mara S Cordoba; Erica C. C. Caldas Rosa; Hulya Kayserili; Virginia Kimonis; Erica Wu; Cecilia Mellado; Vineet Aggarwal; Antonio Richieri-Costa; Décio Brunoni; Talyta M Canó; Alexander A. L Jorge; Chong Ae Kim; Rachel Honjo; Débora R Bertola; Raissa M Dandalo-Girardi; Yavuz Bayram; Alper Gezdirici; Elif Yilmaz-Gulec; Evren Gumus; Gülay C Yilmaz; Nobuhiko Okamoto; Hirofumi Ohashi; Zeynep Coban–Akdemir; Tadahiro Mitani; Shalini N Jhangiani; Donna M Muzny; Neysa A. P Regattieri; Robert Pogue; Rinaldo W Pereira; Paulo A Otto; Richard A Gibbs; Bassam R Ali; Hans van Bokhoven; Han G Brunner; V. Reid Sutton; James R Lupski; Angela M Vianna-Morgante; Claudia M. B Carvalho; Juliana F MazzeuHuman Mutation v. 43, n. 7, p. 900-918, July 2022Hoboken 2022Acesso online. A biblioteca também possui exemplares impressos. |
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Material Type: Artigo
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Back Cover, Volume 43, Issue 7Lima, Ariadne R. ; Ferreira, Barbara M. ; Zhang, Chaofan ; Jolly, Angad ; Du, Haowei ; White, Janson J. ; Dawood, Moez ; Lins, Tulio C. ; Chiabai, Marcela A. ; Beusekom, Ellen ; Cordoba, Mara S. ; Caldas Rosa, Erica C.C. ; Kayserili, Hulya ; Kimonis, Virginia ; Wu, Erica ; Mellado, Cecilia ; Aggarwal, Vineet ; Richieri‐Costa, Antonio ; Brunoni, Décio ; Canó, Talyta M. ; Jorge, Alexander A. L. ; Kim, Chong A. ; Honjo, Rachel ; Bertola, Débora R. ; Dandalo‐Girardi, Raissa M. ; Bayram, Yavuz ; Gezdirici, Alper ; Yilmaz‐Gulec, Elif ; Gumus, Evren ; Yilmaz, Gülay C. ; Okamoto, Nobuhiko ; Ohashi, Hirofumi ; Coban–Akdemir, Zeynep ; Mitani, Tadahiro ; Jhangiani, Shalini N. ; Muzny, Donna M. ; Regattieri, Neysa A.P. ; Pogue, Robert ; Pereira, Rinaldo W. ; Otto, Paulo A. ; Gibbs, Richard A. ; Ali, Bassam R. ; Bokhoven, Hans ; Brunner, Han G. ; Sutton, V. Reid ; Lupski, James R. ; Vianna‐Morgante, Angela M. ; Carvalho, Claudia M. B. ; Mazzeu, Juliana F.Human mutation, 2022-07, Vol.43 (7), p.ii-ii [Periódico revisado por pares]Texto completo disponível |