Polysomy and p16 deletion by fluorescence in situ hybridization in the diagnosis of indeterminate biliary strictures

Gastrointestinal Endoscopy

Volumn 75, Issue 1, 2012, Pages 74-79

  Gonda, Tamas A ^a   Glick, Michael P ^a   Sethi, Amrita ^a   Poneros, John M ^a   Palmas, Walter ^a   Iqbal, Shahzad ^a   Gonzalez, Susana ^a   Nandula, Subhadra V ^a   Emond, Jean C ^a   Brown, Robert S ^a   Murty, Vundavalli V ^a   Stevens, Peter D ^a  

^a NewYork Presbyterian Hospital   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BILE DUCT CARCINOMA; BILE DUCT OBSTRUCTION; CHROMOSOME 9P; CHROMOSOME DELETION; CYTOLOGY; DIAGNOSTIC TEST ACCURACY STUDY; FEMALE; FOLLOW UP; HUMAN; HUMAN TISSUE; IN SITU HYBRIDIZATION; MAJOR CLINICAL STUDY; MALE; POLYSOMY; PRIORITY JOURNAL; SCLEROSING CHOLANGITIS; SCREENING TEST; SENSITIVITY AND SPECIFICITY;

ANEUPLOIDY; AREA UNDER CURVE; BILE DUCT NEOPLASMS; BILE DUCTS, INTRAHEPATIC; CHOLANGIOCARCINOMA; CHOLANGITIS, SCLEROSING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 3; CHROMOSOMES, HUMAN, PAIR 7; CHROMOSOMES, HUMAN, PAIR 9; CONSTRICTION, PATHOLOGIC; CYTODIAGNOSIS; DNA, NEOPLASM; FEMALE; GENES, P16; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; RETROSPECTIVE STUDIES; ROC CURVE;

EID: 84855196461     PISSN: 00165107     EISSN: 10976779     Source Type: Journal    
DOI: 10.1016/j.gie.2011.08.022     Document Type: Article

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