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Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr-381 residue in FGFR2 gene
- Source :
- Clinical Genetics, Clinical Genetics, Wiley, 2014, 85 (6), pp.598--599. 〈10.1111/cge.12213〉, Clinical Genetics, Wiley, 2014, 85 (6), pp.598--599. ⟨10.1111/cge.12213⟩
- Publication Year :
- 2014
- Publisher :
- HAL CCSD, 2014.
-
Abstract
- International audience; no abstract
Details
- Language :
- English
- ISSN :
- 00099163 and 13990004
- Database :
- OpenAIRE
- Journal :
- Clinical Genetics, Clinical Genetics, Wiley, 2014, 85 (6), pp.598--599. 〈10.1111/cge.12213〉, Clinical Genetics, Wiley, 2014, 85 (6), pp.598--599. ⟨10.1111/cge.12213⟩
- Accession number :
- edsair.dedup.wf.001..1ce5dc792b3a55a82cd02e03c4a1a066