[Phenylketonuria undiagnosed, unrecognizable and neglected. Review of failures in diagnosis, therapy, and prevention of hereditary disorders of phenylalanine]. / Fenylketonurie nepoznané, "nepoznatelné" a zanedbané. Prehled neúspechu v diagnostice, lécbe a prevenci dedicných poruch fenylalaninu.
Cesk Pediatr
; 42(3): 134-8, 1987 Mar.
Article
in Cs
| MEDLINE
| ID: mdl-3581266
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phenylketonurias
Type of study:
Diagnostic_studies
Limits:
Humans
/
Infant
/
Newborn
Language:
Cs
Journal:
Cesk Pediatr
Year:
1987
Document type:
Article