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Volumn 3, Issue 2, 2007, Pages 169-181

Hereditary cancer syndrome diagnosis: Molecular genetic clues and cancer control

Author keywords

CDKN2A mutation; Cetuximab; Erlotinib; Familial atypical multiple mole melanoma; Familial atypical multiple mole melanoma syndrome; Hereditary cancer; Lynch syndrome; Melanoma; Monoclonal antibodies; Pancreatic cancer

Indexed keywords

BCR ABL PROTEIN; BEVACIZUMAB; BRCA1 PROTEIN; CETUXIMAB; CYCLIN DEPENDENT KINASE INHIBITOR; CYCLIN DEPENDENT KINASE INHIBITOR 2A; DNA; EPIDERMAL GROWTH FACTOR RECEPTOR 2; ERLOTINIB; EVEROLIMUS; FLUOROURACIL; FOLINIC ACID; GEMCITABINE; IMATINIB; IRINOTECAN; OXALIPLATIN; SORAFENIB; SUNITINIB; TEMSIROLIMUS; TRASTUZUMAB; UNCLASSIFIED DRUG; VASCULOTROPIN; VON HIPPEL LINDAU PROTEIN;

EID: 34247135358     PISSN: 14796694     EISSN: 17448301     Source Type: Journal    
DOI: 10.2217/14796694.3.2.169     Document Type: Article
Times cited : (10)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.