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 Es
| IBECS
| ID: ibc-87152
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
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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