3-years experience review of neonatal screening for hemoglobin disorders using tandem mass spectrometry

Clinica Chimica Acta

Volumn 412, Issue 15-16, 2011, Pages 1476-1479

  Boemer, François ^a   Cornet, Yves ^b   Libioulle, Cécile ^a   Segers, Karin ^a   Bours, Vincent ^a   Schoos, Roland ^a  

^a UNIVERSITY OF LIÈGE   (Belgium)

^b UNIVERSITY OF LIÈGE   (Belgium)

Author keywords

Hemoglobin disorders; Neonatal screening; Tandem mass spectrometry

Indexed keywords

HEMOGLOBIN;

ARTICLE; BELGIUM; BIOTECHNOLOGICAL PROCEDURES; GENE MUTATION; HEMOGLOBIN DETERMINATION; HEMOGLOBINOPATHY; HUMAN; LABORATORY TEST; MAJOR CLINICAL STUDY; NEWBORN; NEWBORN SCREENING; POPULATION RESEARCH; PRIORITY JOURNAL; PROTEIN VARIANT; TANDEM MASS SPECTROMETRY; VALIDITY;

FETAL HEMOGLOBIN; GENOTYPE; HUMANS; INFANT, NEWBORN; METABOLISM, INBORN ERRORS; MUTATION; NEONATAL SCREENING; SENSITIVITY AND SPECIFICITY; TANDEM MASS SPECTROMETRY;

EID: 79956311222     PISSN: 00098981     EISSN: 18733492     Source Type: Journal    
DOI: 10.1016/j.cca.2011.04.031     Document Type: Article

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