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Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia
Barraza-García, J., Rivera-Pedroza, C.I., Hisado-Oliva, A., Belinchón-Martínez, A., Sentchordi-Montané, L., Duncan, E.L., Clark, G.R., del Pozo, A., Ibáñez-Garikano, K., Offiah, A., Prieto-Matos, P.,Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12964
Date:
February, 2017
File:
PDF, 1.66 MB
english, 2017