Phenotypic and mutational spectrum of ROR2-related Robinow syndrome
ROR2相关Robinow综合征的表型和突变谱
期刊:Human Mutation
影响因子:3.7
doi:10.1002/humu.24375
Lima, Ariadne R; Ferreira, Barbara M; Zhang, Chaofan; Jolly, Angad; Du, Haowei; White, Janson J; Dawood, Moez; Lins, Tulio C; Chiabai, Marcela A; van 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; van Bokhoven, Hans; Brunner, Han G; Sutton, V Reid; Lupski, James R; Vianna-Morgante, Angela M; Carvalho, Claudia M B; Mazzeu, Juliana F