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Volumn 4, Issue 1, 2007, Pages

The explosion of hereditary cancer knowledge: Benefiting from a family information service

Author keywords

[No Author keywords available]

Indexed keywords

CANCER RISK; FAMILIAL CANCER; FAMILY HISTORY; GENE MUTATION; GENETIC COUNSELING; GENETIC VARIABILITY; HEALTH SERVICE; HIGH RISK POPULATION; HUMAN; MEDICAL INFORMATION; MOLECULAR GENETICS; PHENOTYPE; REVIEW; RISK ASSESSMENT;

EID: 33847769898     PISSN: 15485315     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1548-5315(11)70017-1     Document Type: Review
Times cited : (2)

References (7)
  • 2
    • 33745528138 scopus 로고    scopus 로고
    • The role of prevention in oncology practice: Results from a 2004 survey of American Society of Clinical Oncology members
    • Ganz PA, Kwan L, Somerfield MR, et al. The role of prevention in oncology practice: results from a 2004 survey of American Society of Clinical Oncology members. J Clin Oncol 2006;24:2948-2957.
    • (2006) J Clin Oncol , vol.24 , pp. 2948-2957
    • Ganz, P.A.1    Kwan, L.2    Somerfield, M.R.3
  • 3
    • 33847780893 scopus 로고    scopus 로고
    • Lynch HT, Snyder C, Lynch J, Ghate S, Thome S. Family information service (FIS) in a BRCA1 extended family. J Clin Oncol 2006;24(18S):1028.
    • Lynch HT, Snyder C, Lynch J, Ghate S, Thome S. Family information service (FIS) in a BRCA1 extended family. J Clin Oncol 2006;24(18S):1028.
  • 4
    • 0028823186 scopus 로고
    • Attenuated familial adenomatous polyposis (AFAP): A phenotypically and genotypically distinctive variant of FAP
    • Lynch HT, Smyrk T, McGinn T, et al. Attenuated familial adenomatous polyposis (AFAP): a phenotypically and genotypically distinctive variant of FAP. Cancer 1995;76:2427-2433.
    • (1995) Cancer , vol.76 , pp. 2427-2433
    • Lynch, H.T.1    Smyrk, T.2    McGinn, T.3
  • 5
    • 0036143702 scopus 로고    scopus 로고
    • Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: The familial atypical multiple mole melanoma-pancreatic carcinoma syndrome
    • Lynch HT, Brand RE, Hogg D, et al. Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical multiple mole melanoma-pancreatic carcinoma syndrome. Cancer 2002;94:84-96.
    • (2002) Cancer , vol.94 , pp. 84-96
    • Lynch, H.T.1    Brand, R.E.2    Hogg, D.3
  • 6
    • 0035864981 scopus 로고    scopus 로고
    • Family information service and hereditary cancer
    • Lynch HT. Family information service and hereditary cancer. Cancer 2001;91:625-628.
    • (2001) Cancer , vol.91 , pp. 625-628
    • Lynch, H.T.1
  • 7
    • 0042327828 scopus 로고    scopus 로고
    • Carrier risk status changes resulting from mutation testing in hereditary nonpolyposis colorectal cancer and hereditary breast-ovarian cancer
    • Watson P, Narod SA, Fodde R, et al. Carrier risk status changes resulting from mutation testing in hereditary nonpolyposis colorectal cancer and hereditary breast-ovarian cancer. Am J Hum Genet 2003;40:591-596.
    • (2003) Am J Hum Genet , vol.40 , pp. 591-596
    • Watson, P.1    Narod, S.A.2    Fodde, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.