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Results: 1
A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene
Authors:
Bretones, P Duprez, L Parma, J David, M Vassart, G Rodien, P
Citation:
P. Bretones et al., A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene, THYROID, 11(10), 2001, pp. 977-980
Risultati:
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