Rapid and specific detection of clinically significant haemoglobinopathies using electrospray mass spectrometry-mass spectrometry

British Journal of Haematology

Volumn 130, Issue 4, 2005, Pages 635-643

  Daniel, Yvonne A ^b,c   Turner, Charles ^a   Haynes, Roberta M ^b   Hunt, Beverley J ^b   Neil Dalton, R ^a  

^a GUY S HOSPITAL   (United Kingdom)

^b ST THOMAS HOSPITAL   (United Kingdom)

^c KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

Haemoglobinopathy; Mass spectrometry; Population screening; Sickle cell disease

Indexed keywords

HAPTOGLOBIN O; HEMOGLOBIN; HEMOGLOBIN AC; HEMOGLOBIN AD; HEMOGLOBIN AE; HEMOGLOBIN AO; HEMOGLOBIN C; HEMOGLOBIN CC; HEMOGLOBIN D; HEMOGLOBIN DD; HEMOGLOBIN E; HEMOGLOBIN EE; HEMOGLOBIN OO; HEMOGLOBIN S; HEMOGLOBIN VARIANT; TRYPSIN; UNCLASSIFIED DRUG; HEMOGLOBIN ARAB; HEMOGLOBIN D PUNJAB;

ARTICLE; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DIAGNOSTIC PROCEDURE; DIAGNOSTIC VALUE; ELECTROSPRAY MASS SPECTROMETRY; ENZYMATIC DEGRADATION; FALSE NEGATIVE RESULT; FALSE POSITIVE RESULT; HEMOGLOBIN AA; HEMOGLOBIN C DISEASE; HEMOGLOBIN SC; HEMOGLOBIN SC DISEASE; HEMOGLOBIN SS; HEMOGLOBINOPATHY; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MASS SPECTROMETRY; MONITORING; NEWBORN SCREENING; PHENOTYPE; PRENATAL SCREENING; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN VARIANT; SCREENING TEST; SENSITIVITY AND SPECIFICITY; SICKLE CELL ANEMIA; SICKLE CELL TRAIT; EVALUATION; GENETICS; METHODOLOGY; MUTATION; NEWBORN;

HEMOGLOBIN C; HEMOGLOBIN, SICKLE; HEMOGLOBINOPATHIES; HEMOGLOBINS; HEMOGLOBINS, ABNORMAL; HETEROZYGOTE; HOMOZYGOTE; HUMANS; INFANT, NEWBORN; MUTATION; NEONATAL SCREENING; SENSITIVITY AND SPECIFICITY; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION;

EID: 24944506479     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2005.05646.x     Document Type: Article

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