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
Med. clín (Ed. impr.)
; 136(7): 313-314, mar. 2011. ilus
Article
in Spanish
| IBECS
| ID: ibc-87152
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
No disponible
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Collection:
National databases
/
Spain
Health context:
Sustainable Health Agenda for the Americas
Health problem:
Goal 1 Equitable access to health services
Database:
IBECS
Main subject:
Steroid 21-Hydroxylase
/
Adrenal Hyperplasia, Congenital
/
Molecular Diagnostic Techniques
Type of study:
Diagnostic study
/
Screening study
Limits:
Female
/
Humans
/
Male
/
Infant, Newborn
Language:
Spanish
Journal:
Med. clín (Ed. impr.)
Year:
2011
Document type:
Article
Institution/Affiliation country:
Hospital Universitario Infantil Gregorio Marañón/España
/
Universdiad Autónoma de Madrid/España
/
Universidad Autónoma/España