The Orphanet Rare Diseases Ontology (ORDO) : a reference tool integrating clinical and genetic data. A. Rath*, A. Olry*, C. Gonthier*, L. Chanas*, H. Parkinson**, J. Malone**, D. Vasant**, M. Hanauer*, B. Urbero*, S. Ay - Dysplasia - Document - PDFSEARCH.IO

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Date: 2014-05-02 11:54:43 Genetic genealogy Congenital disorders Spondyloepimetaphyseal dysplasia Rare diseases Spondyloepiphyseal dysplasia congenita Osteochondrodysplasia Dysplasia Pseudoachondroplasia Multiple epiphyseal dysplasia Health Medicine Collagen disease		The Orphanet Rare Diseases Ontology (ORDO) : a reference tool integrating clinical and genetic data. A. Rath, A. Olry, C. Gonthier, L. Chanas, H. Parkinson, J. Malone, D. Vasant*, M. Hanauer, B. Urbero*, S. Ay Add to Reading List Source URL: www.rare-diseases.eu Download Document from Source Website File Size: 1,88 MB Share Document on Facebook