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Clinical features of non-classical 21-hydroxylase deficiency after normal newborn mass screening.
Takahashi, Funa; Adachi, Shuhei; Sakurai, Nodoka; Mori, Toshihiko; Fujikura, Kaori; Usui, Takeshi; Hasegawa, Tomonobu.
Afiliação
  • Takahashi F; Department of Pediatrics, NTT EAST Medical Center Sapporo, Sapporo, Japan.
  • Adachi S; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.
  • Sakurai N; Department of Pediatrics, NTT EAST Medical Center Sapporo, Sapporo, Japan.
  • Mori T; Department of Pediatrics, NTT EAST Medical Center Sapporo, Sapporo, Japan.
  • Fujikura K; Sapporo City Institute of Public Health, Sapporo, Japan.
  • Usui T; Department of Medical Genetics, Shizuoka General Hospital, Shizuoka, Japan.
  • Hasegawa T; Shizuoka Graduate University of Public Health, Shizuoka, Japan.
Pediatr Int ; 65(1): e15674, 2023.
Article em En | MEDLINE | ID: mdl-38009625
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans / Newborn Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans / Newborn Idioma: En Ano de publicação: 2023 Tipo de documento: Article