Brain Transcriptome Database (BrainTx)http://rdf.ncbi.nlm.nih.gov/pubmed/

M. Oldridge, et.al., Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B., Nature genetics, 2000, 24
http://rdf.ncbi.nlm.nih.gov/pubmed/10700182

M. Oldridge, et.al., Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B., Nature genetics, 2000, 24

http://rdf.ncbi.nlm.nih.gov/pubmed/

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