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Genotypic spectrum of 21-hydroxylase deficiency in an endogamous population.
Mahmoud, R A A; Amr, N H; Toaima, N N; Kamal, T M; Elsedfy, H H.
Afiliação
  • Mahmoud RAA; Department of Pediatrics, Ain Shams University, Children's Hospital, Abbassiah Square, Cairo, Egypt. dr.ranahakim@med.asd.edu.eg.
  • Amr NH; Department of Pediatrics, Ain Shams University, Children's Hospital, Abbassiah Square, Cairo, Egypt.
  • Toaima NN; Department of Pediatrics, Ain Shams University, Children's Hospital, Abbassiah Square, Cairo, Egypt.
  • Kamal TM; Genetics Unit, Department of Pediatrics, Ain Shams University, Cairo, Egypt.
  • Elsedfy HH; Department of Pediatrics, Ain Shams University, Children's Hospital, Abbassiah Square, Cairo, Egypt.
J Endocrinol Invest ; 45(2): 347-359, 2022 Feb.
Article em En | MEDLINE | ID: mdl-34341969
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Virilismo / Desequilíbrio Hidroeletrolítico / Cortisona / Esteroide 21-Hidroxilase / Hiperplasia Suprarrenal Congênita Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Virilismo / Desequilíbrio Hidroeletrolítico / Cortisona / Esteroide 21-Hidroxilase / Hiperplasia Suprarrenal Congênita Idioma: En Ano de publicação: 2022 Tipo de documento: Article