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Progression of genetic study in idiopathic hypogonadotropic hypogonadism / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism ; (12): 244-248, 2012.
Artigo em Chinês | WPRIM | ID: wpr-425110
ABSTRACT
Idiopathic hypogonadotropic hypogonadism(IHH) is a complex oligogenic disease.About 60% of patients are associated with anosmia or hyposmia,also known as Kallmann syndrome. Based on genetic and molecular biological research,about more than ten IHH responsible genes have been discovered.

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Idioma: Chinês Revista: Chinese Journal of Endocrinology and Metabolism Ano de publicação: 2012 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Idioma: Chinês Revista: Chinese Journal of Endocrinology and Metabolism Ano de publicação: 2012 Tipo de documento: Artigo