Author:
Ben-Shachar S,Khajavi M,Withers MA,Shaw CA,van Bokhoven H,Brunner HG,Lupski JR
Subject
Genetics(clinical),Genetics
Reference32 articles.
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2. Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome;van Bokhoven;Nat Genet,2000
3. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2;Afzal;Nat Genet,2000
4. Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B;Oldridge;Nat Genet,2000
5. Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B;Schwabe;Am J Hum Genet,2000
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