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Update on the Swedish Newborn Screening for Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
Zetterström, Rolf H; Karlsson, Leif; Falhammar, Henrik; Lajic, Svetlana; Nordenström, Anna.
Affiliation
  • Zetterström RH; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, SE-171 76 Stockholm, Sweden.
  • Karlsson L; Department of Molecular Medicine and Surgery, Karolinska Institutet, SE-171 76 Stockholm, Sweden.
  • Falhammar H; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, SE-171 76 Stockholm, Sweden.
  • Lajic S; Department of Women's and Children's Health, Karolinska Institutet, SE-171 76 Stockholm, Sweden.
  • Nordenström A; Department of Molecular Medicine and Surgery, Karolinska Institutet, SE-171 76 Stockholm, Sweden.
Int J Neonatal Screen ; 6(3)2020 Aug 28.
Article in En | MEDLINE | ID: mdl-33239597
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Prognostic_studies / Screening_studies Language: En Journal: Int J Neonatal Screen Year: 2020 Document type: Article Affiliation country: Suecia Country of publication: Suiza
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Prognostic_studies / Screening_studies Language: En Journal: Int J Neonatal Screen Year: 2020 Document type: Article Affiliation country: Suecia Country of publication: Suiza