Associated Papers
A novel variant in the ROR2 gene underlying brachydactyly type B: a case report.
Shao J et al.
Bmc Pediatrics, 2022
A new mutation in the gene ROR2 causes brachydactyly type B1.
Huang D et al.
Gene, 2014
[Mutation analysis of the pathogenic gene in a Chinese family with Brachydactyly type B1].
Li CM et al.
Yi Chuan = Hereditas, 2011
A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes.
Schwarzer W et al.
Human Molecular Genetics, 2009
Cloning and expression pattern of chicken Ror2 and functional characterization of truncating mutations in Brachydactyly type B and Robinow syndrome.
Stricker S et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists, 2006
Brachydactyly type B1: report of a family with de novo ROR2 mutation.
Hamamy H et al.
Clinical Genetics, 2006
[Genetic analysis of the UGT1A1 gene mutation sites in a Chinese family suffered from Gilbert's syndrome].
Yu LH et al.
Yi Chuan = Hereditas, 2006
[Identification of a recurrent mutation in the ROR2 gene in a Chinese family with brachydactyly type B].
Yang W et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2004
One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.
Afzal AR et al.
Human Mutation, 2003
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.
Schwabe GC et al.
American Journal of Human Genetics, 2000
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