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Utilidad del análisis molecular en el diagnóstico diferencial del déficit congénito de 21-hidroxilasa detectado en el cribado neonatal / Usefulness of molecular analysis in the differential diagnosis of congenital 21-hidroxylase deficiency detected in neonatal screening
Soriano Guillén, Leandor; Velázquez De Cuelar Paracchi, María; Ezquieta, Begoña.
Affiliation
  • Soriano Guillén, Leandor; Universdiad Autónoma de Madrid. Fundación Jiménez Díaz. Unidad de Endocrinología Infantil. Madrid. España
  • Velázquez De Cuelar Paracchi, María; Universidad Autónoma. Fundación Jiménez Díaz. Servicio de Pediatría. Madrid. España
  • Ezquieta, Begoña; Hospital Universitario Infantil Gregorio Marañón. Laboratorio de Diagn´sotico Molecular. Madrid. España
Med. clín (Ed. impr.) ; 136(7): 313-314, mar. 2011. ilus
Article in Es | IBECS | ID: ibc-87152
Responsible library: ES1.1
Localization: BNCS
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Subject(s)
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Collection: 06-national / ES Database: IBECS Main subject: Steroid 21-Hydroxylase / Adrenal Hyperplasia, Congenital / Molecular Diagnostic Techniques Type of study: Diagnostic_studies / Screening_studies Limits: Female / Humans / Male / Newborn Language: Es Journal: Med. clín (Ed. impr.) Year: 2011 Document type: Article
Search on Google
Add to My VHL
Print
XML
Collection: 06-national / ES Database: IBECS Main subject: Steroid 21-Hydroxylase / Adrenal Hyperplasia, Congenital / Molecular Diagnostic Techniques Type of study: Diagnostic_studies / Screening_studies Limits: Female / Humans / Male / Newborn Language: Es Journal: Med. clín (Ed. impr.) Year: 2011 Document type: Article