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Volumn 18, Issue 15, 2012, Pages 4213-

Lifetime cancer risks of PTEN mutation carriers - Letter

Author keywords

[No Author keywords available]

Indexed keywords

CANCER GENETICS; CANCER RISK; CANCER SUSCEPTIBILITY; FOLLOW UP; GENE; GENE MUTATION; GENETIC CORRELATION; HETEROZYGOSITY; HUMAN; LETTER; MALIGNANT NEOPLASTIC DISEASE; MEDICAL RESEARCH; PHENOTYPE; PRIORITY JOURNAL; PROMOTER REGION; PTEN GENE; PUBLICATION;

EID: 84864434719     PISSN: 10780432     EISSN: 15573265     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-12-0577     Document Type: Letter
Times cited : (6)

References (5)
  • 2
    • 78650908302 scopus 로고    scopus 로고
    • A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands
    • Tan MH, Mester J, Peterson C, Yang Y, Chen JL, Rybicki LA, et al. A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands. Am J Hum Genet 2011;88:42-56.
    • (2011) Am J Hum Genet , vol.88 , pp. 42-56
    • Tan, M.H.1    Mester, J.2    Peterson, C.3    Yang, Y.4    Chen, J.L.5    Rybicki, L.A.6
  • 3
    • 79958071334 scopus 로고    scopus 로고
    • Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome
    • Bonadona V, Bonaiti B, Olschwang S, Grandjouan S, Huiart L, Longy M, et al. Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. JAMA 2011;305:2304-10.
    • (2011) JAMA , vol.305 , pp. 2304-2310
    • Bonadona, V.1    Bonaiti, B.2    Olschwang, S.3    Grandjouan, S.4    Huiart, L.5    Longy, M.6
  • 4
    • 84860605783 scopus 로고    scopus 로고
    • Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: A prospective cohort study
    • Win AK, Young JP, Lindor NM, Tucker KM, Ahnen DJ, Young GP, et al. Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study. J Clin Oncol 2012;30:958-64.
    • (2012) J Clin Oncol , vol.30 , pp. 958-964
    • Win, A.K.1    Young, J.P.2    Lindor, N.M.3    Tucker, K.M.4    Ahnen, D.J.5    Young, G.P.6
  • 5
    • 42149139456 scopus 로고    scopus 로고
    • ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007
    • DOI 10.1097/GIM.0b013e31816b5cae, PII 0012581720080400000009
    • Richards CS, Bale S, Bellissimo DB, Das S, GrodyWW, Hegde MR, et al. ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007. Genet Med 2008;10:294-300. (Pubitemid 351544132)
    • (2008) Genetics in Medicine , vol.10 , Issue.4 , pp. 294-300
    • Richards, C.S.1    Bale, S.2    Bellissimo, D.B.3    Das, S.4    Grody, W.W.5    Hegde, M.R.6    Lyon, E.7    Ward, B.E.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.