Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency

Vieira, Teresa C; Boldarine, Valter T; Abucham, Julio.
Arq. bras. endocrinol. metab ; 51(7): 1097-1103, out. 2007. tab
Artículo en Inglés | LILACS | ID: lil-470073

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