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Volumn 24, Issue 7, 2011, Pages 954-962

Frequency, molecular pathology and potential clinical significance of partial chromosome 3 aberrations in uveal melanoma

Author keywords

eye neoplasms; molecular genetics; uveal melanoma

Indexed keywords

ADULT; AGED; ALLELIC IMBALANCE; ARTICLE; CHROMOSOME 3; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CYTOGENETICS; FEMALE; FOLLOW UP; GENOTYPE; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; MALE; METASTASIS; MICROSATELLITE MARKER; MOLECULAR PATHOLOGY; MONOSOMY; MONOSOMY 3; PARTIAL CHROMOSOME 3 ALTERATION; PATHOGENESIS; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; UVEA MELANOMA;

EID: 79959973290     PISSN: 08933952     EISSN: 15300285     Source Type: Journal    
DOI: 10.1038/modpathol.2011.51     Document Type: Article
Times cited : (29)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.