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Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene.
Leccese, A; Longo, V; Dimatteo, C; De Girolamo, G; Trunzo, R; D'Andrea, G; Bafunno, V; Margaglione, M; Santacroce, R.
Afiliação
  • Leccese A; Department of Clinical and Experimental Medicine, University of Foggia, Italy. Electronic address: leccese.angelica@tiscali.it.
  • Longo V; Department of Clinical and Experimental Medicine, University of Foggia, Italy.
  • Dimatteo C; Department of Clinical and Experimental Medicine, University of Foggia, Italy.
  • De Girolamo G; Department of Clinical and Experimental Medicine, University of Foggia, Italy.
  • Trunzo R; Department of Clinical and Experimental Medicine, University of Foggia, Italy.
  • D'Andrea G; Department of Clinical and Experimental Medicine, University of Foggia, Italy.
  • Bafunno V; Department of Clinical and Experimental Medicine, University of Foggia, Italy.
  • Margaglione M; Department of Clinical and Experimental Medicine, University of Foggia, Italy.
  • Santacroce R; Department of Clinical and Experimental Medicine, University of Foggia, Italy.
Clin Chim Acta ; 437: 48-51, 2014 Nov 01.
Article em En | MEDLINE | ID: mdl-25025300
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Esteroide 21-Hidroxilase / Hiperplasia Suprarrenal Congênita / Genótipo Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans / Middle aged Idioma: En Revista: Clin Chim Acta Ano de publicação: 2014 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: Fenótipo / Esteroide 21-Hidroxilase / Hiperplasia Suprarrenal Congênita / Genótipo Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans / Middle aged Idioma: En Revista: Clin Chim Acta Ano de publicação: 2014 Tipo de documento: Article