Neonatal screening: From the 'Guthrie age' to the 'genetic age'

Journal of Inherited Metabolic Disease

Volumn 30, Issue 4, 2007, Pages 418-422

  Dhondt, Jean Louis ^a  

^a Centre Hospitalier Saint Philibert GHICL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYPROGESTERONE;

CONFERENCE PAPER; CONGENITAL ADRENAL HYPERPLASIA; COST EFFECTIVENESS ANALYSIS; CYSTIC FIBROSIS; DIET THERAPY; DNA MICROARRAY; ENZYME THERAPY; ETHNIC DIFFERENCE; GENETIC ANALYSIS; GENETIC VARIABILITY; HEALTH PROGRAM; HUMAN; HYPERPHENYLALANINEMIA; INBORN ERROR OF METABOLISM; INFORMED CONSENT; LYSOSOME STORAGE DISEASE; MEDICAL ETHICS; MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE DEFICIENCY; MENTAL DEFICIENCY; NEWBORN; NEWBORN SCREENING; PARENTAL ATTITUDE; PATIENT MONITORING; PHENYLKETONURIA; PUBLIC HEALTH SERVICE; TANDEM MASS SPECTROMETRY;

FAMILY HEALTH; HISTORY, 20TH CENTURY; HISTORY, 21ST CENTURY; HUMANS; INFANT, NEWBORN; METABOLISM, INBORN ERRORS; NEONATAL SCREENING; PHENYLKETONURIAS;

EID: 34548510123     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-007-0624-9     Document Type: Conference Paper

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