Author:
Schwarzer Wibke,Witte Florian,Rajab Anna,Mundlos Stefan,Stricker Sigmar
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Reference22 articles.
1. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2;Afzal;Nat. Genet.,2000
2. Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B;Oldridge;Nat. Genet.,2000
3. Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B;Schwabe;Am. J. Hum. Genet.,2000
4. Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome;van Bokhoven;Nat. Genet.,2000
5. One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B;Afzal;Hum. Mutat.,2003
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