Author:
Huang Dan,Jiang Shujuan,Zhang Yuanyuan,Liu Xiaoliang,Zhang Jiubin,He Rong
Subject
Genetics,General Medicine
Reference30 articles.
1. One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B;Afzal;Hum. Mutat.,2003
2. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2;Afzal;Nat. Genet.,2000
3. The deleted in brachydactyly B domain of ROR2 is required for receptor activation by recruitment of Src;Akbarzadeh;PLoS One,2008
4. ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome;Bacchelli;Clin. Genet.,2003
5. Ror2, encoding a receptor-like tyrosine kinase, is required for cartilage and growth plate development;DeChiara;Nat. Genet.,2000
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