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A study of the clinical and radiological features in a cohort of 93 patients with aCOL2A1mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype

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Description scientific article published on 21 January 2015
Author/s

author: Geert Mortier  Valérie Cormier-Daire  Marianne Rohrbach  Emma Wakeling  Annick Toutain  Andrew Green  Raoul Hennekam  Annemarie H van der Hout  Allan M Lund  Hermine E Veenstra-Knol 

Publication date January 21, 2015
Language English
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