✦ LIBER ✦
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B
✍ Scribed by Oldridge, Michael; M Fortuna, Ana; Maringa, Monika; Propping, Peter; Mansour, Sahar; Pollitt, Christine; DeChiara, Thomas M.; Kimble, Robert B.; Valenzuela, David M.; Yancopoulos, George D.
- Book ID
- 109827762
- Publisher
- Nature Publishing Group
- Year
- 2000
- Tongue
- English
- Weight
- 558 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1061-4036
- DOI
- 10.1038/73495
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