Dominant Mutations in Ror2, Encoding an Orphan Receptor Tyrosine Kinase, Cause Brachydactyly Type B

AuthID
 P-001-0R7
11
Author(s)
Oldridge, M
·
Fortuna, AM
·
Propping, P
·
Mansour, S
·
Pollitt, C
·
Kimble, RB
·
Valenzuela, DM
·
Yancopoulos, GD
·
Wilkie, AOM
Tipo de Documento
Article
Year published
2000
Publicado
in NATURE GENETICS, ISSN: 1061-4036
Volume: 24, Número: 3, Páginas: 275-278 (4)
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Publication Identifiers
Pubmed: 10700182
SCOPUS: 2-s2.0-0034009511
Wos: WOS:000085590600019
Source Identifiers
ISSN: 1061-4036
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