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Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations
Ramos, H. E., Carre, A., Chevrier, L., Szinnai, G., Tron, E., Cerqueira, T. L. O., Leger, J., Cabrol, S., Puel, O., Queinnec, C., De Roux, N., Guillot, L., Castanet, M., Polak, M.Volume:
171
Language:
english
Journal:
European Journal of Endocrinology
DOI:
10.1530/eje-13-1006
Date:
September, 2014
File:
PDF, 268 KB
english, 2014