Please use this identifier to cite or link to this item: http://dl.umsu.ac.ir/handle/Hannan/48131
Title: TBX6 null variants and a common hypomorphic allele in congenital scoliosis
Authors: Wu, N;Ming, X;Xiao, J;Wu, Z;Chen, X;Shinawi, M;Shen, Y;Yu, G;Liu, J;Xie, H;Gucev, Z S;Liu, S;Yang, N;Al-Kateb, H;Chen, J;Zhang, J;Hauser, N;Zhang, T;Tasic, V;Liu, P;Su, X;Pan, X;Liu, C;Wang, L;Shen, J;Shen, J;Chen, Y;Zhang, T;Zhang, J;Choy, K W;Wang, J;Wang, Q;Li, S;Zhou, W;Guo, J;Wang, Y;Zhang, C;Zhao, Hong;An, Yu;Zhao, Yu;Wang, J;Liu, Z;Zuo, Y;Tian, Y;Weng, X;Sutton, V R;Wang, H;Ming, Y;Kulkarni, S;Zhong, T P;Giampietro, P F;Dunwoodie, S L;Cheung, S W;Zhang, X;Jin, L;Lupski, J R;Qiu, G;Zhang, F
Year: 22-Jan-2015
Abstract: Congenital scoliosis is a common type of vertebral malformation. Genetic susceptibility has been implicated in congenital scoliosis.
URI: http://dl.umsu.ac.ir/handle/Hannan/48131
ISSN: 10.1056/NEJMoa1406829
Appears in Collections:New England Journal of Medicine2015

Files in This Item:
File Description SizeFormat 
341.pdf1.28 MBAdobe PDFThumbnail
Download    Request a copy


Items in HannanDL are protected by copyright, with all rights reserved, unless otherwise indicated.