"Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B". Nat. Genet. 24 (3): 275-8. March 2000. doi:10.1038/73495. PMID10700182.
"Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B". Nat. Genet. 24 (3): 275-8. March 2000. doi:10.1038/73495. PMID10700182.