메뉴 건너뛰기




Volumn 23, Issue 6, 2010, Pages 388-400

Genetic testing and prevention of hereditary cancer at the MMCI - Over 10 years of experience

Author keywords

Genes; Genetic testing; Hereditary cancer; Prevention; Syndromes

Indexed keywords

BRCA1 ASSOCIATED RING DOMAIN PROTEIN 1; BRCA2 PROTEIN; CYCLIN DEPENDENT KINASE INHIBITOR 2A; PROTEIN MLH1; PROTEIN MSH2; PROTEIN MSH6;

EID: 78650664925     PISSN: 0862495X     EISSN: 18025307     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (10)

References (58)
  • 2
    • 0032730774 scopus 로고    scopus 로고
    • Genetic susceptibility to non-polyposis colorectal cancer
    • Lynch HT, de la Chapelle A. Genetic susceptibility to non-polyposis colorectal cancer. J Med Genet 1999; 36(11): 801-818.
    • (1999) J Med Genet , vol.36 , Issue.11 , pp. 801-818
    • Lynch, H.T.1    De La Chapelle, A.2
  • 3
    • 0034330224 scopus 로고    scopus 로고
    • Lynch syndrome: Genetics, natural history, genetic counseling, and prevention
    • Lynch HT, Lynch J. Lynch syndrome: genetics, natural history, genetic counseling, and prevention. J Clin Oncol 2000;18(Suppl):19S-31S.
    • (2000) J Clin Oncol , vol.18 , Issue.SUPPL.
    • Lynch, H.T.1    Lynch, J.2
  • 4
    • 0027248156 scopus 로고
    • Genetics, natural history, tumor spectrum and patology of hereditary non-polyposis colorectal cancer: An updated review
    • Lynch HT, Smyrk TC, Watson P et al. Genetics, natural history, tumor spectrum and patology of hereditary non-polyposis colorectal cancer: an updated review. Gastroenterology 1993; 104:1535-1549.
    • (1993) Gastroenterology , vol.104 , pp. 1535-1549
    • Lynch, H.T.1    Smyrk, T.C.2    Watson, P.3
  • 5
    • 0037422027 scopus 로고    scopus 로고
    • Hereditary colorectal cancer
    • Lynch HT, Chapelle A. Hereditary colorectal cancer. N Eng J Med 2003; 348(10): 919-932.
    • (2003) N Eng J Med , vol.348 , Issue.10 , pp. 919-932
    • Lynch, H.T.1    Chapelle, A.2
  • 6
    • 0028113345 scopus 로고
    • A strong candidate for the breast and ovarian cancer susceptibility gene
    • Miki Y, Swensen J, Shattuck-Eldens D et al. A strong candidate for the breast and ovarian cancer susceptibility gene. Science 1994; 266(5182): 66-71.
    • (1994) Science , vol.266 , Issue.5182 , pp. 66-71
    • Miki, Y.1    Swensen, J.2    Shattuck-Eldens, D.3
  • 7
    • 0006713602 scopus 로고
    • Identification of the breast cancer susceptibility gene BRCA2
    • Wooster R, Bignell G, Lancaster J et al. Identification of the breast cancer susceptibility gene BRCA2. Nature 1995; 378(6559): 789-792.
    • (1995) Nature , vol.378 , Issue.6559 , pp. 789-792
    • Wooster, R.1    Bignell, G.2    Lancaster, J.3
  • 8
    • 0022506980 scopus 로고
    • A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarkoma
    • Friend SH, Bernards R, Rogelj S. A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarkoma. Nature 1986; 323(6089): 643-646.
    • (1986) Nature , vol.323 , Issue.6089 , pp. 643-646
    • Friend, S.H.1    Bernards, R.2    Rogelj, S.3
  • 9
    • 0026254581 scopus 로고
    • Testing for germline p53 mutations in cancer families
    • Li FP, Correa P, Fraumeni JF jr. Testing for germline p53 mutations in cancer families. Cancer Epidemiol Biomark Prev 1991; 1:91-94.
    • (1991) Cancer Epidemiol Biomark Prev , vol.1 , pp. 91-94
    • Li, F.P.1    Correa, P.2
  • 10
    • 0025648762 scopus 로고
    • Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome
    • Srivastava S, Zou Z, Pirrollo K et al. Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome. Nature 1990; 348(6303): 747-749.
    • (1990) Nature , vol.348 , Issue.6303 , pp. 747-749
    • Srivastava, S.1    Zou, Z.2    Pirrollo, K.3
  • 11
    • 33751027938 scopus 로고    scopus 로고
    • Hereditary aetiology of cancer diseases and the importance of genetic counselling and testing in oncology
    • Goetz P, Foretova L, Puchmajerova A. Hereditary aetiology of cancer diseases and the importance of genetic counselling and testing in oncology. Klin Onkol 2006; 19 (Suppl)-44-48
    • (2006) Klin Onkol , vol.19 , pp. 44-48
    • Goetz, P.1    Foretova, L.2    Puchmajerova, A.3
  • 12
    • 13744263782 scopus 로고    scopus 로고
    • Hereditary cancer predisposition syndromes
    • Garber JE, Offit K. Hereditary cancer predisposition syndromes. J Clin Oncol 2005; 23(2): 276-292
    • (2005) J Clin Oncol , vol.23 , Issue.2 , pp. 276-292
    • Garber, J.E.1    Offit, K.2
  • 13
    • 33645745489 scopus 로고    scopus 로고
    • Genetic and preventive services for hereditary breast and ovarian cancer in the Czech Republic
    • Foretová L, Petráková K, Palácová M et al. Genetic and preventive services for hereditary breast and ovarian cancer in the Czech Republic. Hereditary Cancer in Clinical Practice 2006; 4(1): 3-6.
    • (2006) Hereditary Cancer in Clinical Practice , vol.4 , Issue.1 , pp. 3-6
    • Foretová, L.1    Petráková, K.2    Palácová, M.3
  • 14
    • 17344365851 scopus 로고    scopus 로고
    • Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
    • Ford D, Easton DF, Stratton M et al. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet 1998; 62(3): 676-689.
    • (1998) Am J Hum Genet , vol.62 , Issue.3 , pp. 676-689
    • Ford, D.1    Easton, D.F.2    Stratton, M.3
  • 15
    • 77952981208 scopus 로고    scopus 로고
    • Hereditary breast and ovarian cancer (HBOC): Clinical features and Counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li.-Fraumeni
    • Shulman LP. Hereditary breast and ovarian cancer (HBOC): Clinical features and Counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li.-Fraumeni. Obstet Gynecol Clin N Am 2010; 37(1): 109-133.
    • Obstet Gynecol Clin N Am 2010 , vol.37 , Issue.1 , pp. 109-133
    • Shulman, L.P.1
  • 16
    • 77951206427 scopus 로고    scopus 로고
    • Triple-negative breast cancer: Molecular features, pathogenesis, treatment and current lines of research
    • Bosch A, Eroles P, Zaragoza R et al. Triple-negative breast cancer: Molecular features, pathogenesis, treatment and current lines of research. Cancer Treatment Reviews 2010; 36(3): 206-215.
    • (2010) Cancer Treatment Reviews , vol.36 , Issue.3 , pp. 206-215
    • Bosch, A.1    Eroles, P.2    Zaragoza, R.3
  • 17
    • 68149163711 scopus 로고    scopus 로고
    • Triple-negative breast cancers are increased in black women regardless of age or body mass index
    • Stead LA, Lash TL, Sobieraj JE et al Triple-negative breast cancers are increased in black women regardless of age or body mass index. Breast Cancer Research 2009; 11:R18.
    • (2009) Breast Cancer Research , vol.11
    • Stead, L.A.1    Lash, T.L.2    Sobieraj, J.E.3
  • 20
    • 0038036629 scopus 로고    scopus 로고
    • The recommendation of clinical care for patients with breast and ovarian cancer and for healthy people with germline mutations in BRCA and BRCA2 genes
    • Bartoňková H, Foretová L, Helmichová E et al. The recommendation of clinical care for patients with breast and ovarian cancer and for healthy people with germline mutations In BRCA] and BRCA2 genes. KIm Onkol 2003; 16(1): 28-34.
    • (2003) KIm Onkol , vol.16 , Issue.1 , pp. 28-34
    • Bartoňková, H.1    Foretová, L.2    Helmichová, E.3
  • 21
    • 78650642385 scopus 로고    scopus 로고
    • Syndrom hereditárního karcinomu prsu a ovarií
    • Plevová P, Novotný J, Petráková K et al. Syndrom hereditárního karcinomu prsu a ovarií. Klin Onkol 2009 (Suppl S1):S6-S11.
    • (2009) Klin Onkol , Issue.SUPPL. S1
    • Plevová, P.1    Novotný, J.2    Petráková, K.3
  • 22
    • 77954654101 scopus 로고    scopus 로고
    • Population based study of BRCA 1/2 mutations: Family history based criteria identify minority of mutation carriers
    • Mateju J, Stribrna M, Zikan M et al. Population based study of BRCA 1/2 mutations: family history based criteria identify minority of mutation carriers. Neoplasma 2010; 57(3): 280-285.
    • (2010) Neoplasma , vol.57 , Issue.3 , pp. 280-285
    • Mateju, J.1    Stribrna, M.2    Zikan, M.3
  • 23
    • 8844220451 scopus 로고    scopus 로고
    • CHEK2 is a multiorgan cancer susceptibility gene
    • Cybulski C, Górskl T, Huzarski T et al. CHEK2 is a multiorgan cancer susceptibility gene. Am J Hum Genet 2004; 75(6):1131-1135.
    • (2004) Am J Hum Genet , vol.75 , Issue.6 , pp. 1131-1135
    • Cybulski, C.1    Górskl, T.2    Huzarski, T.3
  • 24
    • 3042582651 scopus 로고    scopus 로고
    • CHEK2 1100delC and susceptibility to breast cancer. a collaborative analysis involving 10, 860 breast cancer cases and 9,065 controls from 10 studies
    • The CHEK2 Breast Cancer Case-Control Consortium
    • The CHEK2 Breast Cancer Case-Control Consortium. CHEK2 1100delC and susceptibility to breast cancer. a collaborative analysis involving 10, 860 breast cancer cases and 9,065 controls from 10 studies. Am J Hum Genet 2004; 74(6): 1175-1182.
    • (2004) Am J Hum Genet , vol.74 , Issue.6 , pp. 1175-1182
  • 25
    • 33645084562 scopus 로고    scopus 로고
    • Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer
    • Walsh T, Casadei S, Coats KH et al. Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 In families at high risk of breast cancer. JAMA 2006; 295(12): 1379-1388.
    • (2006) JAMA , vol.295 , Issue.12 , pp. 1379-1388
    • Walsh, T.1    Casadei, S.2    Coats, K.H.3
  • 26
    • 44949263899 scopus 로고    scopus 로고
    • Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer
    • Machackova E, Foretova L, Lukesova M et al. Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer. BMC Cancer 2008, 8(140): 12.
    • (2008) BMC Cancer , vol.8 , Issue.140 , pp. 12
    • Machackova, E.1    Foretova, L.2    Lukesova, M.3
  • 27
    • 66349115872 scopus 로고    scopus 로고
    • Diagnostic guidelines for High-Resolution Melting curve (HRM) analysis: A validation of BRCA1 mutation scanning using the 96-well LightScanner
    • Stoep N, Paridon Ch, Janssens T et al Diagnostic guidelines for High-Resolution Melting curve (HRM) analysis: A validation of BRCA1 mutation scanning using the 96-well LightScanner. Human Mutation 2009; 30(6): 899-909.
    • (2009) Human Mutation , vol.30 , Issue.6 , pp. 899-909
    • Stoep, N.1    Paridon, C.2    Janssens, T.3
  • 28
    • 2342516899 scopus 로고    scopus 로고
    • BRCA1 and BRCA2 mutations in women with familial or early-onset breast/ovarian cancer in the Czech Republic
    • Foretova L, Machackova E, Navratilova M et al. BRCA1 and BRCA2 mutations in women with familial or early-onset breast/ovarian cancer in the Czech Republic. Human Mutation 2004; 23(4): 397-398.
    • (2004) Human Mutation , vol.23 , Issue.4 , pp. 397-398
    • Foretova, L.1    Machackova, E.2    Navratilova, M.3
  • 29
    • 34347223992 scopus 로고    scopus 로고
    • High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic
    • Vasickova P, Machackova E, Lukesova M et al. High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic. BMC Med Genet 2007; 8:32.
    • (2007) BMC Med Genet , vol.8 , pp. 32
    • Vasickova, P.1    Machackova, E.2    Lukesova, M.3
  • 30
    • 48549084778 scopus 로고    scopus 로고
    • A syngeneic variance library for functional annotation of human variation: Application to BRCA2
    • Hucl T, Rago C, Gallmeier E et al. A syngeneic variance library for functional annotation of human variation: application to BRCA2. Cancer Res 2008; 68(13): 5023-5030.
    • (2008) Cancer Res , vol.68 , Issue.13 , pp. 5023-5030
    • Hucl, T.1    Rago, C.2    Gallmeier, E.3
  • 31
    • 20244378377 scopus 로고    scopus 로고
    • The CHEK2 c.1100delC germline mutation rarely contributes to breast cancer development in the Czech Republic
    • Kleibl Z, Novotny J, Bezdickova D et al. The CHEK2 c.1100delC germline mutation rarely contributes to breast cancer development in the Czech Republic. Breast Cancer Research and Treatment 2005; 90(2): 165-167.
    • (2005) Breast Cancer Research and Treatment , vol.90 , Issue.2 , pp. 165-167
    • Kleibl, Z.1    Novotny, J.2    Bezdickova, D.3
  • 32
    • 78650630880 scopus 로고    scopus 로고
    • Magnetic resonance of breast as a screening method in women with high risk of breast cancer
    • Schneiderova M, Belanova R, Lidakova J et al. Magnetic resonance of breast as a screening method In women with high risk of breast cancer. Educational Proceedings. BOD 2009:91-92.
    • (2009) Educational Proceedings. BOD , pp. 91-92
    • Schneiderova, M.1    Belanova, R.2    Lidakova, J.3
  • 33
    • 33751045766 scopus 로고    scopus 로고
    • Breast magnetic resonance imaging in surveillance of women at high risk for breast cancer
    • Schneiderova M, Bartonkova H. Breast magnetic resonance imaging in surveillance of women at high risk for breast cancer. Klin Onkol 2006; 19 (Suppl): 91-96.
    • (2006) Klin Onkol , vol.19 , Issue.SUPPL. , pp. 91-96
    • Schneiderova, M.1    Bartonkova, H.2
  • 34
    • 71049170380 scopus 로고    scopus 로고
    • Penetrance estimated for BRCA1 and BRCA2 based on genetic testing in a clinical cancer genetics service setting: Risk of breast/ovarian cancer quoted should reflect the cancer burden in the family
    • Evans DG, Shenton A, Woodward E. Penetrance estimated for BRCA1 and BRCA2 based on genetic testing in a clinical cancer genetics service setting: Risk of breast/ovarian cancer quoted should reflect the cancer burden in the family. BMC Cancer 2008; 8:155.
    • (2008) BMC Cancer , vol.8 , pp. 155
    • Evans, D.G.1    Shenton, A.2    Woodward, E.3
  • 35
    • 0034236361 scopus 로고    scopus 로고
    • Prophylactic surgery for women at high risk for breast cancer
    • Blanchard DK, Hartmann LC. Prophylactic surgery for women at high risk for breast cancer. Clin Breast Cancer 2000; 1(2): 127-134.
    • (2000) Clin Breast Cancer , vol.1 , Issue.2 , pp. 127-134
    • Blanchard, D.K.1    Hartmann, L.C.2
  • 36
    • 0034017713 scopus 로고    scopus 로고
    • Prophylactic surgery in women with a hereditary predisposition to breast and ovarian cancer 2000
    • Eisen A Rebbeck TR, Wood WC et al. Prophylactic Surgery in Women With a Hereditary Predisposition to Breast and Ovarian Cancer 2000; J Clin Oncol 2000; 18(9): 1980-1995.
    • (2000) J Clin Oncol , vol.18 , Issue.9 , pp. 1980-1995
    • Rebbeck Tr, E.A.1    Wood, W.C.2
  • 37
    • 0033452876 scopus 로고    scopus 로고
    • Prophylactic mastectomy and inherited predisposition to breast carcinoma
    • Hughes KS, Papa MZ, Whitney T et al. Prophylactic mastectomy and inherited predisposition to breast carcinoma. Cancer Supplement 1999; 86:2502-2515.
    • (1999) Cancer Supplement , vol.86 , pp. 2502-2515
    • Hughes, K.S.1    Papa, M.Z.2    Whitney, T.3
  • 38
    • 0034631316 scopus 로고    scopus 로고
    • Presymptomatic DNA testing and prophylactic surgery in families with a BRCA1 or BRCA2 mutation
    • Meijers-Heijboer EJ, Verhoog LC, Brekelmans CTM et al. Presymptomatic DNA testing and prophylactic surgery In families with a BRCA1 or BRCA2 mutation. Lancet 2000; 355(9220): 2015-2020.
    • (2000) Lancet , vol.355 , Issue.9220 , pp. 2015-2020
    • Meijers-Heijboer, E.J.1    Verhoog, L.C.2    Brekelmans, C.T.M.3
  • 39
    • 0035913275 scopus 로고    scopus 로고
    • Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation
    • Meijers-Heijboer H, van Geel B, van Putten WU et al. Breast cancer after prophylactic bilateral mastectomy In women with a BRCA1 or BRCA2 mutation. N Engl J Med 2001;345:159-163.
    • (2001) N Engl J Med , vol.345 , pp. 159-163
    • Meijers-Heijboer, H.1    Van Geel, B.2    Van Putten, W.U.3
  • 40
    • 33751048090 scopus 로고    scopus 로고
    • Prophylactic mastectomy and its Indications in high-risk women
    • Drazan L Prophylactic mastectomy and its Indications In high-risk women Klin Onkol 2006; 19 (Suppl): 97-100.
    • (2006) Klin Onkol , vol.19 , pp. 97-100
    • Drazan, L.1
  • 41
    • 68649097351 scopus 로고    scopus 로고
    • Oboustranná rekonstrukce prsů dvěma DIEP laloky: Jak ji hodnoti pacientky?
    • Dražan L, Hýža R Stupka I et al. Oboustranná rekonstrukce prsů dvěma DIEP laloky: Jak ji hodnoti pacientky? Praktický lékař 2009; 89(6): 306-311.
    • (2009) Praktický Lékař , vol.89 , Issue.6 , pp. 306-311
    • Dražan, L.1    Stupka I, H.R.2
  • 42
    • 0033166374 scopus 로고    scopus 로고
    • A practical approach to familial and hereditary colorectal cancer
    • Ivanovich JL, Reed TE, Ciske DJ et al. A practical approach to familial and hereditary colorectal cancer. Am J Med 1999; 107(1)-68-77.
    • (1999) Am J Med , vol.107 , Issue.1 , pp. 68-77
    • Ivanovich, J.L.1    Reed, T.E.2    Ciske, D.J.3
  • 43
    • 33751060446 scopus 로고    scopus 로고
    • Plevová R Diagnostika Lynchova syndromu - Nové geny a metody
    • Křepelová A, Pavlíková K, Plevová R Diagnostika Lynchova syndromu - nové geny a metody. Klin Onkol 2006; 19 (Suppl): 76-81.
    • (2006) Klin Onkol , vol.19 , Issue.SUPPL. , pp. 76-81
    • Křepelová, A.1    Pavlíková, K.2
  • 44
    • 67650872601 scopus 로고    scopus 로고
    • Hereditární nepolypózní kolorektá lní karcinom (HNPCC, Lynchův syndrom)
    • Plevová P, Novotný J, Šachlová M et al. Hereditární nepolypózní kolorektální karcinom (HNPCC, Lynchův syndrom). Klin Onkol 2009; (Suppl S1): S12-S15.
    • (2009) Klin Onkol , Issue.SUPPL. S1
    • Plevová, P.1    Novotný, J.2    Šachlová, M.3
  • 45
    • 0032522623 scopus 로고    scopus 로고
    • Multiple primary cancers in familles with Li-Fraumenl syndrome
    • Hisada M, Garber JE, Fung CY et al. Multiple primary cancers in familles with Li-Fraumenl syndrome. J Natl Cancer Inst 1998; 90(8)- 606-611.
    • (1998) J Natl Cancer Inst , vol.90 , Issue.8 , pp. 606-611
    • Hisada, M.1    Garber, J.E.2    Fung, C.Y.3
  • 47
    • 33751053516 scopus 로고    scopus 로고
    • Kasuistiky Li-Fraumeni syndromu: Diagnostické a preventivní možnosti
    • Foretová L, Navrátilová M, Petrákova K. Kasuistiky Li-Fraumeni syndromu: diagnostické a preventivní možnosti. Klin Onkol 2006; 19 (Suppl): 85-87
    • (2006) Klin Onkol , vol.19 , Issue.SUPPL. , pp. 85-87
    • Foretová, L.1    Navrátilová, M.2    Petrákova, K.3
  • 49
    • 67650921129 scopus 로고    scopus 로고
    • Syndrom familiárního melanomu (s dysplastickými naevy či bez nich)
    • Foretová L, Macháčková E, Šachlová M et al. Syndrom familiárního melanomu (s dysplastickými naevy či bez nich). Kim Onkol 2009; (Suppl S1): S32-S33.
    • (2009) Kim Onkol , Issue.SUPPL. S1
    • Foretová, L.1    Macháčková, E.2    Šachlová, M.3
  • 53
    • 0034464147 scopus 로고    scopus 로고
    • Very high risk of cancer in familial Peutz-Jeghers syndrome
    • Giardiello FM, Brenslnger JD, Tersmett AC et al. Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 2000; 119(6): 1447-1453.
    • (2000) Gastroenterology , vol.119 , Issue.6 , pp. 1447-1453
    • Giardiello, F.M.1    Brenslnger, J.D.2    Tersmett, A.C.3
  • 55
    • 77956412331 scopus 로고    scopus 로고
    • MUTYH-associated polyposls-variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations
    • Morak M, Laner A, Bacher U et al. MUTYH-associated polyposls-variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations. Clim Genet 2010; 78(4): 353-363.
    • (2010) Clim Genet , vol.78 , Issue.4 , pp. 353-363
    • Morak, M.1    Laner, A.2    Bacher, U.3
  • 56
    • 77956326790 scopus 로고    scopus 로고
    • Genome-wide association studies of cancer predisposition
    • Stadler ZK, Vijai J, Thom P et al Genome-wide association studies of cancer predisposition. Hematol Oncol Clin N Am 2010; 24:973-996.
    • (2010) Hematol Oncol Clin N Am , Issue.24 , pp. 973-996
    • Stadler, Z.K.1    Vijai, J.2    Thom, P.3
  • 57
    • 77956305912 scopus 로고    scopus 로고
    • Inherited predisposition to cancer. Introduction and overview
    • Robson M, Offit K. Inherited predisposition to cancer. Introduction and overview. Hematol Oncol Clin N Am 2010, 24(5):793-797.
    • (2010) Hematol Oncol Clin N Am , vol.24 , Issue.5 , pp. 793-797
    • Robson, M.1    Offit, K.2
  • 58
    • 67349222061 scopus 로고    scopus 로고
    • Breast cancer susceptibility: Current knowledge and implications for genetic counselling
    • Ripperger T, Gadzicki D, Meindl A et al. Breast cancer susceptibility: current knowledge and implications for genetic counselling Eur J Hum Genet 2009; 17(6): 722-731.
    • (2009) Eur J Hum Genet , vol.17 , Issue.6 , pp. 722-731
    • Ripperger, T.1    Gadzicki, D.2    Meindl, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.