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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.
Affiliation
  • 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 in En | MEDLINE | ID: mdl-34341969
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virilism / Water-Electrolyte Imbalance / Cortisone / Steroid 21-Hydroxylase / Adrenal Hyperplasia, Congenital Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Child / Female / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: J Endocrinol Invest Year: 2022 Document type: Article Affiliation country: Egipto
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virilism / Water-Electrolyte Imbalance / Cortisone / Steroid 21-Hydroxylase / Adrenal Hyperplasia, Congenital Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Child / Female / Humans / Infant / Male Country/Region as subject: Africa Language: En Journal: J Endocrinol Invest Year: 2022 Document type: Article Affiliation country: Egipto