## Abstract Robinow syndrome (RS) is a human dwarfism syndrome characterized by mesomelic limb shortening, vertebral and craniofacial malformations and small external genitals. We have analyzed __Ror2__^__‐/‐__^ mice as a model for the developmental pathology of RS. Our results demonstrate that ver
✦ LIBER ✦
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome
✍ Scribed by Brunner, Han G.; van Bokhoven, Hans; Celli, Jacopo; Kayserili, Hülya; van Beusekom, Ellen; Balci, Sevim; Brussel, Wim; Skovby, Flemming; Kerr, Bronwyn; Percin, E. Ferda; Akarsu, Nurten
- Book ID
- 109828672
- Publisher
- Nature Publishing Group
- Year
- 2000
- Tongue
- English
- Weight
- 319 KB
- Volume
- 25
- Category
- Article
- ISSN
- 1061-4036
- DOI
- 10.1038/78113
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