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Diverse growth hormone receptor gene mutations in Laron syndrome
ArticleAbstract: To better understand the molecular genetic basis and genetic epidemiology of Laron syndrome (growth-Palabras claves:Autores:Argente J., Berg M.A., Chernausek S., Francke U., Gracia R., Hopp M., Jaime Guevara-Aguirre, Pérez‐Jurado L., Rosenbloom A.L., Toledo S.Fuentes:scopusImmunoblot studies of the acid-labile subunit (ALS) in biological fluids, normal human serum and in children with GH deficiency and GH receptor deficiency before and after long-term therapy with GH or IGF-I respectively
ArticleAbstract: OBJECTIVE: The aims of this investigation were (a) to study the presence of immunoreactive forms ofPalabras claves:Autores:Argente J., Gargosky S.E., Jaime Guevara-Aguirre, Labarta J., Lee P., Rosenfeld R.G., Simpson D.Fuentes:scopus