Moat, Stuart J <br/><br/>
Newborn blood spot screening for sickle cell disease by using tandem mass spectrometry: implementation of a protocol to identify only the disease states of sickle cell disease.  [electronic resource] 

 -  Clinical chemistry  Feb 2014 
 - 373-80 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1530-8561 
<br/><br/><label>Standard No.: </label>10.1373/clinchem.2013.210948  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anemia, Sickle Cell--blood<br/>Blood Specimen Collection<br/>Chromatography, High Pressure Liquid--methods<br/>Genetic Testing--methods<br/>Genetic Variation<br/>Hemoglobin, Sickle--genetics<br/>Hemoglobins, Abnormal--genetics<br/>Humans<br/>Infant, Newborn<br/>Isoelectric Focusing<br/>Neonatal Screening--methods<br/>Peptide Fragments--analysis<br/>Sensitivity and Specificity<br/>Sickle Cell Trait--blood<br/>Tandem Mass Spectrometry--methods<br/>Trypsin--chemistry