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Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes
Weh, E., Reis, L.M., Tyler, R.C., Bick, D., Rhead, W.J., Wallace, S., McGregor, T.L., Dills, S.K., Chao, M.-C., Murray, J.C., Semina, E.V.Volume:
86
Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12241
Date:
August, 2014
File:
PDF, 668 KB
english, 2014