E-mail

E-mail a Wiley Online Library Link

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

Article first published online: 20 FEB 2013 | DOI: 10.1111/cge.12088

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field

SEARCH