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Volumn 59, Issue 11, 2013, Pages 1672-1674
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Point-of-care and over-thecounter qualitative human chorionic gonadotropin (hcg) devices remain susceptible to false-negative results caused by excess HCG β core fragment
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Author keywords
[No Author keywords available]
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Indexed keywords
CHORIONIC GONADOTROPIN BETA SUBUNIT;
CHORIONIC GONADOTROPIN;
DIAGNOSTIC KIT;
FALSE NEGATIVE RESULT;
GYNECOLOGICAL AND OBSTETRIC GENERAL EQUIPMENT;
HUMAN;
LETTER;
OVER THE COUNTER DEVICE;
POINT OF CARE DEVICE;
POINT OF CARE TESTING;
PREGNANCY RAPID TEST;
PREGNANCY TEST;
PRENATAL CARE;
URINALYSIS;
DEVICES;
DIAGNOSTIC KIT;
FEMALE;
HOSPITAL INFORMATION SYSTEM;
LABORATORY DIAGNOSIS;
STANDARDS;
URINE;
EQUIPMENT;
STANDARD;
CHORIONIC GONADOTROPIN;
CHORIONIC GONADOTROPIN, BETA SUBUNIT, HUMAN;
FALSE NEGATIVE REACTIONS;
FEMALE;
HUMANS;
POINT-OF-CARE SYSTEMS;
PREGNANCY TESTS;
REAGENT KITS, DIAGNOSTIC;
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EID: 84887057082
PISSN: 00099147
EISSN: 15308561
Source Type: Journal
DOI: 10.1373/clinchem.2013.212795 Document Type: Letter |
Times cited : (12)
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References (4)
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