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pro vyhledávání: '"Lerario M. Antonio"'
Autor:
Berenice B. Mendonca, Alexander A. L. Jorge, Luciani R. Carvalho, Ivo J.P. Arnhold, Mariana F A Funari, Martha K.P. Huayllas, Lerario M. Antonio, Anna Flavia Figueredo Benedetti, Fernanda A. Correa, Lucas Santos de Santana, Mirta Miras, Ricardo V Perez, Marilena Nakaguma
Publikováno v:
Journal of the Endocrine Society
Background: Congenital GH deficiency (GHD) can be isolated (IGHD) or combined with other pituitary hormone deficiencies (CPHD). The identification of mutations has clinical implications for the management of patients and genetic counseling. Objective