SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Dan Huang, Shujuan Jiang, Yuanyuan Zhang, Xiaoliang Liu, Jiubin Zhang, Rong He, A new mutation in the gene ROR2 causes brachydactyly type B1, Gene, 2014, 547, 1, 106

    CrossRef

  2. 2
    Cong-Min LI, Feng-Yu WANG, Wei-Wei SUN, Shu-Li HAN, Ming-Xiu CHANG, Hui-Gen FENG, Mutation analysis of the pathogenic gene in a Chinese family with Brachydactyly type B1, Hereditas (Beijing), 2011, 33, 2, 147

    CrossRef

  3. 3
    Natalia Lyashenko, Martina Weissenböck, Amnon Sharir, Reinhold G. Erben, Yasuhiro Minami, Christine Hartmann, Mice lacking the orphan receptor ror1 have distinct skeletal abnormalities and are growth retarded, Developmental Dynamics, 2010, 239, 8
  4. 4
    Dan Lv, Yang Luo, Wei Yang, Lihua Cao, Yaran Wen, Xiuli Zhao, Miao Sun, Wilson H-Y Lo, Xue Zhang, A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family, Journal of Human Genetics, 2009, 54, 7, 422

    CrossRef