Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.
Oldridge M; Fortuna AM; Maringa M; Propping P; Mansour S; Pollitt C; DeChiara TM; Kimble RB; Valenzuela DM; Yancopoulos GD; Wilkie AO; Nature Genetics, 2000, vol. 24, issue 3, p 275, ISSN 10614036. ISBN 10614036.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef