T. M. Dechiara
AuthID: R-00G-JJR
1
TITLE: Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B Full Text
AUTHORS: Oldridge, M; Fortuna, AM; Maringa, M; Propping, P; Mansour, S; Pollitt, C; DeChiara, TM; Kimble, RB; Valenzuela, DM; Yancopoulos, GD; Wilkie, AOM;
PUBLISHED: 2000, SOURCE: NATURE GENETICS, VOLUME: 24, ISSUE: 3
AUTHORS: Oldridge, M; Fortuna, AM; Maringa, M; Propping, P; Mansour, S; Pollitt, C; DeChiara, TM; Kimble, RB; Valenzuela, DM; Yancopoulos, GD; Wilkie, AOM;
PUBLISHED: 2000, SOURCE: NATURE GENETICS, VOLUME: 24, ISSUE: 3
