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AO Caglayan, H Per, G Akgumus, H Gumus, J Baranoski, M Canpolat, M Calik, A Yikilmaz, K Bilguvar, S Kumandas and M Gunel Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum Clinical Genetics 84

Version of Record online: 20 FEB 2013 | DOI: 10.1111/cge.12088

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