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Volumn 124, Issue 5, 2016, Pages 317-323

Clinical performance of the Food and Drug Administration-Approved high-risk HPV test for the detection of high-grade cervicovaginal lesions

Author keywords

College of American Pathologists (CAP) benchmark; cotesting; high grade cervicovaginal lesion; human papillomavirus (HPV) test; Papanicolaou (Pap) test

Indexed keywords

ADENOCARCINOMA IN SITU; ADOLESCENT; ADULT; AGED; ARTICLE; CYTODIAGNOSIS; DIAGNOSTIC TEST ACCURACY STUDY; FALSE NEGATIVE RESULT; FEMALE; FOLLOW UP; HUMAN; HUMAN PAPILLOMAVIRUS DNA TEST; MAJOR CLINICAL STUDY; PAPANICOLAOU TEST; PRECANCER; PRIORITY JOURNAL; RETROSPECTIVE STUDY; UTERINE CERVIX BIOPSY; UTERINE CERVIX CANCER; UTERINE CERVIX CARCINOMA; UTERINE CERVIX CARCINOMA IN SITU; UTERINE CERVIX CYTOLOGY; UTERINE CERVIX DYSPLASIA; VAGINA SMEAR KIT; CERVICAL INTRAEPITHELIAL NEOPLASIA; FOOD AND DRUG ADMINISTRATION; GENETICS; ISOLATION AND PURIFICATION; MIDDLE AGED; PAPILLOMAVIRIDAE; PAPILLOMAVIRUS INFECTIONS; PROCEDURES; UNITED STATES; UTERINE CERVICAL NEOPLASMS; VAGINA SMEAR; VAGINAL NEOPLASMS; VERY ELDERLY; VIROLOGY; YOUNG ADULT;

EID: 84968560966     PISSN: 1934662X     EISSN: 19346638     Source Type: Journal    
DOI: 10.1002/cncy.21687     Document Type: Article
Times cited : (45)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.