Your browser doesn't support javascript.
loading
Congenital adrenal hyperplasia with homozygous and heterozygous mutations: a rare family case report.
Cheng, Tiantian; Liu, Jing; Sun, Wenwen; Song, Guangyao; Ma, Huijuan.
Afiliação
  • Cheng T; Department of Internal Medicine, School of Clinical Medicine, North China University of Science and Technology, Tangshan, 063210, Hebei, China.
  • Liu J; Department of Endocrinology and Metabolic Diseases, Hebei General Hospital, Shijiazhuang, 050051, Hebei, China.
  • Sun W; Department of Endocrinology and Metabolic Diseases, Hebei General Hospital, Shijiazhuang, 050051, Hebei, China.
  • Song G; Department of Internal Medicine, School of Clinical Medicine, North China University of Science and Technology, Tangshan, 063210, Hebei, China.
  • Ma H; Department of Endocrinology and Metabolic Diseases, Hebei General Hospital, Shijiazhuang, 050051, Hebei, China.
BMC Endocr Disord ; 22(1): 57, 2022 Mar 07.
Article em En | MEDLINE | ID: mdl-35255871
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esteroide 21-Hidroxilase / Hiperplasia Suprarrenal Congênita / Heterozigoto / Homozigoto / Mutação Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Adult / Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esteroide 21-Hidroxilase / Hiperplasia Suprarrenal Congênita / Heterozigoto / Homozigoto / Mutação Tipo de estudo: Diagnostic_studies / Etiology_studies Limite: Adult / Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article