메뉴 건너뛰기




Volumn 132, Issue 3 I, 1998, Pages 389-397

Childhood cancer predisposition: Applications of molecular testing and future implications

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER GENETICS; CANCER SUSCEPTIBILITY; CHILD; CHILDHOOD CANCER; FAMILIAL CANCER; GENE MUTATION; GENETIC ANALYSIS; GENETIC PREDISPOSITION; GENETIC SCREENING; HUMAN; MOLECULAR GENETICS; ONCOGENE; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0031940725     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(98)70007-1     Document Type: Article
Times cited : (21)

References (74)
  • 1
    • 0028051414 scopus 로고
    • The genetics of childhood cancer
    • D Malkin C Portwine The genetics of childhood cancer Eur J Cancer 30 1994 1942 1946
    • (1994) Eur J Cancer , vol.30 , pp. 1942-1946
    • Malkin, D1    Portwine, C2
  • 2
    • 0027181632 scopus 로고
    • The role of gene mutations in the genesis of familial cancers
    • C Eng BAJ Ponder The role of gene mutations in the genesis of familial cancers FASEB J 7 1993 910 919
    • (1993) FASEB J , vol.7 , pp. 910-919
    • Eng, C1    Ponder, BAJ2
  • 3
    • 0028796840 scopus 로고
    • Concordance for Hodgkin's disease in identical twins suggesting genetic susceptibility to the young-adult form of the disease
    • TM Mack W Cozen DK Shibata LM Weiss BN Nathwani AM Hernandez Concordance for Hodgkin's disease in identical twins suggesting genetic susceptibility to the young-adult form of the disease N Engl J Med 332 1995 413 418
    • (1995) N Engl J Med , vol.332 , pp. 413-418
    • Mack, TM1    Cozen, W2    Shibata, DK3    Weiss, LM4    Nathwani, BN5    Hernandez, AM6
  • 4
    • 8944224533 scopus 로고    scopus 로고
    • Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2
    • CY Ho B Otterud RD Legare T Varvil R Saxena DB DeHart Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2 Blood 87 1996 5218 5224
    • (1996) Blood , vol.87 , pp. 5218-5224
    • Ho, CY1    Otterud, B2    Legare, RD3    Varvil, T4    Saxena, R5    DeHart, DB6
  • 5
    • 0014422255 scopus 로고
    • Deaths from childhood cancer in sibs
    • RW Miller Deaths from childhood cancer in sibs N Engl J Med 279 1968 122 126
    • (1968) N Engl J Med , vol.279 , pp. 122-126
    • Miller, RW1
  • 6
    • 0029679636 scopus 로고    scopus 로고
    • Are we ready to screen for inherited susceptibility to cancer?
    • NA Holtzman Are we ready to screen for inherited susceptibility to cancer? Oncology 10 1996 57 64
    • (1996) Oncology , vol.10 , pp. 57-64
    • Holtzman, NA1
  • 7
    • 0030563202 scopus 로고    scopus 로고
    • Pitfalls of genetic testing
    • R Hubbard RC Lewontin Pitfalls of genetic testing N Engl J Med 334 1996 1192 1193
    • (1996) N Engl J Med , vol.334 , pp. 1192-1193
    • Hubbard, R1    Lewontin, RC2
  • 8
    • 0029011024 scopus 로고
    • Genetic testing of the common cancers: potential and problems
    • BAJ Ponder Genetic testing of the common cancers: potential and problems Eur J Cancer 31 1995 807 808
    • (1995) Eur J Cancer , vol.31 , pp. 807-808
    • Ponder, BAJ1
  • 9
    • 0026074818 scopus 로고
    • Cooperation between oncogenes
    • T Hunter Cooperation between oncogenes Cell 64 1991 249 270
    • (1991) Cell , vol.64 , pp. 249-270
    • Hunter, T1
  • 10
    • 0026010995 scopus 로고
    • Molecular themes in oncogenesis
    • JM Bishop Molecular themes in oncogenesis Cell 64 1991 235 248
    • (1991) Cell , vol.64 , pp. 235-248
    • Bishop, JM1
  • 11
    • 0027231568 scopus 로고
    • Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
    • LM Mulligan JBJ Kwok CS Healey MJ Elsdon C Eng E Gardner Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A Nature 363 1993 458 460
    • (1993) Nature , vol.363 , pp. 458-460
    • Mulligan, LM1    Kwok, JBJ2    Healey, CS3    Elsdon, MJ4    Eng, C5    Gardner, E6
  • 13
    • 0028199074 scopus 로고
    • Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC
    • LM Mulligan C Eng CS Healey D Clayton JBJ Kwok E Gardner Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC Nat Genet 6 1994 70 74
    • (1994) Nat Genet , vol.6 , pp. 70-74
    • Mulligan, LM1    Eng, C2    Healey, CS3    Clayton, D4    Kwok, JBJ5    Gardner, E6
  • 14
    • 0028174024 scopus 로고
    • A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
    • RMW Hofstra RM Landsvater I Ceccherini RP Stulp T Stelwagen Y Lou A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma Nature 367 1994 375 376
    • (1994) Nature , vol.367 , pp. 375-376
    • Hofstra, RMW1    Landsvater, RM2    Ceccherini, I3    Stulp, RP4    Stelwagen, T5    Lou, Y6
  • 15
    • 0026059515 scopus 로고
    • Tumor suppressor genes
    • CJ Marshall Tumor suppressor genes Cell 64 1991 313 326
    • (1991) Cell , vol.64 , pp. 313-326
    • Marshall, CJ1
  • 16
    • 0015043748 scopus 로고
    • Mutation and cancer: statistical study of retinoblastoma
    • AG Knudson Mutation and cancer: statistical study of retinoblastoma Proc Natl Acad Sci U S A 68 1971 820 823
    • (1971) Proc Natl Acad Sci U S A , vol.68 , pp. 820-823
    • Knudson, AG1
  • 17
    • 0027742295 scopus 로고
    • The human mutator homolog MSH2 and its association with hereditary nonpolyposis colon cancer
    • R Fishel MK Lescoe MRS Rao NG Copeland NA Jenkins J Garber The human mutator homolog MSH2 and its association with hereditary nonpolyposis colon cancer Cell 75 1993 1027 1038
    • (1993) Cell , vol.75 , pp. 1027-1038
    • Fishel, R1    Lescoe, MK2    Rao, MRS3    Copeland, NG4    Jenkins, NA5    Garber, J6
  • 18
    • 0027145633 scopus 로고
    • Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
    • FS Leach NC Nicolaides N Papadopoulos B Liu J Jen R Parsons Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer Cell 75 1993 1215 1225
    • (1993) Cell , vol.75 , pp. 1215-1225
    • Leach, FS1    Nicolaides, NC2    Papadopoulos, N3    Liu, B4    Jen, J5    Parsons, R6
  • 19
    • 0028221943 scopus 로고
    • Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer
    • CE Bronner SM Baker PT Morrison G Warren LG Smith MK Lescoe Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer Nature 368 1994 258 261
    • (1994) Nature , vol.368 , pp. 258-261
    • Bronner, CE1    Baker, SM2    Morrison, PT3    Warren, G4    Smith, LG5    Lescoe, MK6
  • 20
    • 0028106776 scopus 로고
    • hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds
    • B Liu RE Parsons SR Hamilton G Peterson HT Lynch P Watson hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds Cancer Res 54 1994 4590 4594
    • (1994) Cancer Res , vol.54 , pp. 4590-4594
    • Liu, B1    Parsons, RE2    Hamilton, SR3    Peterson, G4    Lynch, HT5    Watson, P6
  • 21
    • 2942569549 scopus 로고    scopus 로고
    • Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients
    • B Liu R Parsons N Papadopoulos NC Nicolaides HT Lynch P Watson Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients Nat Med 2 1996 169 174
    • (1996) Nat Med , vol.2 , pp. 169-174
    • Liu, B1    Parsons, R2    Papadopoulos, N3    Nicolaides, NC4    Lynch, HT5    Watson, P6
  • 22
    • 0027933070 scopus 로고
    • Mutations of two PMS homologues in hereditary nonpolyposis colon cancer
    • NC Nicolaides N Papadopoulos B Liu Y-F Wei KC Carter SM Ruben Mutations of two PMS homologues in hereditary nonpolyposis colon cancer Nature 371 1994 75 80
    • (1994) Nature , vol.371 , pp. 75-80
    • Nicolaides, NC1    Papadopoulos, N2    Liu, B3    Wei, Y-F4    Carter, KC5    Ruben, SM6
  • 23
    • 0024595101 scopus 로고
    • Detection of polymorphisms of human DNA by gel electrophoresis as single strand conformation polymorphisms
    • M Orita H Iwahana H Kanazawa K Hayashi T Sekiya Detection of polymorphisms of human DNA by gel electrophoresis as single strand conformation polymorphisms Proc Natl Acad Sci U S A 86 1989 2766 2770
    • (1989) Proc Natl Acad Sci U S A , vol.86 , pp. 2766-2770
    • Orita, M1    Iwahana, H2    Kanazawa, H3    Hayashi, K4    Sekiya, T5
  • 27
    • 0027430658 scopus 로고
    • Screening patients for heterozygous p53 mutations using a functional assay in yeast
    • C Ishioka T Frebourg Y-X Yan M Vidal SH Friend S Schmidt Screening patients for heterozygous p53 mutations using a functional assay in yeast Nat Genet 5 1993 124 129
    • (1993) Nat Genet , vol.5 , pp. 124-129
    • Ishioka, C1    Frebourg, T2    Yan, Y-X3    Vidal, M4    Friend, SH5    Schmidt, S6
  • 28
    • 0027078647 scopus 로고
    • A functional screen for germ line p53 mutations based on transcriptional activation
    • T Frebourg N Barbier J Kassell Y-S Ng P Romero SH Friend A functional screen for germ line p53 mutations based on transcriptional activation Cancer Res 52 1992 6976 6978
    • (1992) Cancer Res , vol.52 , pp. 6976-6978
    • Frebourg, T1    Barbier, N2    Kassell, J3    Ng, Y-S4    Romero, P5    Friend, SH6
  • 29
    • 0029684565 scopus 로고    scopus 로고
    • Genetics of retinoblastoma: implications for other human cancers
    • DW Yandell C Poremba Genetics of retinoblastoma: implications for other human cancers Med Pediatr Oncol 1 Suppl 1996 25 28
    • (1996) Med Pediatr Oncol , vol.1 , Issue.Suppl , pp. 25-28
    • Yandell, DW1    Poremba, C2
  • 30
    • 0022623369 scopus 로고
    • Second primary neoplasms in patients with retinoblastoma
    • GJ Draper BM Sanders JE Kingston Second primary neoplasms in patients with retinoblastoma Br J Cancer 53 1986 661 671
    • (1986) Br J Cancer , vol.53 , pp. 661-671
    • Draper, GJ1    Sanders, BM2    Kingston, JE3
  • 32
    • 0022506980 scopus 로고
    • A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
    • SH Friend R Bernards S Rogelj RA Weinberg JM Rapaport DM Albert A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma Nature 323 1986 643 646
    • (1986) Nature , vol.323 , pp. 643-646
    • Friend, SH1    Bernards, R2    Rogelj, S3    Weinberg, RA4    Rapaport, JM5    Albert, DM6
  • 33
    • 0023473012 scopus 로고
    • Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein
    • SH Friend JM Horowitz MR Gerber X-F Wang E Bogenmann FP Li Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein Proc Natl Acad Sci U S A 84 1987 9059 9063
    • (1987) Proc Natl Acad Sci U S A , vol.84 , pp. 9059-9063
    • Friend, SH1    Horowitz, JM2    Gerber, MR3    Wang, X-F4    Bogenmann, E5    Li, FP6
  • 34
    • 0029033861 scopus 로고
    • The retinoblastoma protein and cell cycle control
    • RA Weinberg The retinoblastoma protein and cell cycle control Cell 81 1995 323 330
    • (1995) Cell , vol.81 , pp. 323-330
    • Weinberg, RA1
  • 36
    • 0028907719 scopus 로고
    • Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and nonhereditary retinoblastoma
    • V Blanquet C Turleau MS Gross-Morand C Senamaud-Beaufort F Doz C Besmond Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and nonhereditary retinoblastoma Hum Mol Genet 4 1995 383 388
    • (1995) Hum Mol Genet , vol.4 , pp. 383-388
    • Blanquet, V1    Turleau, C2    Gross-Morand, MS3    Senamaud-Beaufort, C4    Doz, F5    Besmond, C6
  • 37
    • 0014587529 scopus 로고
    • Soft-tissue sarcomas, breast cancer, and other neoplasms: A familial syndrome?
    • FP Li JF Fraumeni Soft-tissue sarcomas, breast cancer, and other neoplasms: A familial syndrome? Ann Intern Med 71 1969 747 752
    • (1969) Ann Intern Med , vol.71 , pp. 747-752
    • Li, FP1    Fraumeni, JF2
  • 38
    • 0028149189 scopus 로고
    • Li-Fraumeni syndrome [review]
    • JM Birch Li-Fraumeni syndrome [review] Eur J Cancer 30 1994 1935 1941
    • (1994) Eur J Cancer , vol.30 , pp. 1935-1941
    • Birch, JM1
  • 39
    • 0020045180 scopus 로고
    • Prospective study of a family cancer syndrome
    • FP Li JF Fraumeni Prospective study of a family cancer syndrome JAMA 247 1982 2692 2694
    • (1982) JAMA , vol.247 , pp. 2692-2694
    • Li, FP1    Fraumeni, JF2
  • 40
    • 0026578534 scopus 로고
    • The Li-Fraumeni syndrome: from clinical epidemiology to molecular genetics
    • LC Strong WR Williams MA Tainsky The Li-Fraumeni syndrome: from clinical epidemiology to molecular genetics Am J Epidemiol 135 1991 190 194
    • (1991) Am J Epidemiol , vol.135 , pp. 190-194
    • Strong, LC1    Williams, WR2    Tainsky, MA3
  • 41
    • 0025633582 scopus 로고
    • Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
    • D Malkin FP Li LC Strong JF Fraumeni CE Nelson DH Kim Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms Science 250 1990 1233 1238
    • (1990) Science , vol.250 , pp. 1233-1238
    • Malkin, D1    Li, FP2    Strong, LC3    Fraumeni, JF4    Nelson, CE5    Kim, DH6
  • 43
    • 0026669469 scopus 로고
    • p53 function and dysfunction
    • B Vogelstein KW Kinzler p53 function and dysfunction Cell 70 1992 523 526
    • (1992) Cell , vol.70 , pp. 523-526
    • Vogelstein, B1    Kinzler, KW2
  • 44
    • 0028087776 scopus 로고
    • p53, guardian of Rb
    • E White p53, guardian of Rb Nature 371 1994 21 22
    • (1994) Nature , vol.371 , pp. 21-22
    • White, E1
  • 45
    • 0026525839 scopus 로고
    • Prevalence and spectrum of germline mutations in the p53 gene among patients with sarcoma
    • J Toguchida T Yamaguchi SH Dayton RL Beauchamp GE Herrera K Ishizaki Prevalence and spectrum of germline mutations in the p53 gene among patients with sarcoma N Engl J Med 326 1992 1301 1308
    • (1992) N Engl J Med , vol.326 , pp. 1301-1308
    • Toguchida, J1    Yamaguchi, T2    Dayton, SH3    Beauchamp, RL4    Herrera, GE5    Ishizaki, K6
  • 46
    • 0028958465 scopus 로고
    • Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma
    • L Diller E Sexsmith A Gottlieb FP Li D Malkin Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma J Clin Invest 95 1995 1606 1611
    • (1995) J Clin Invest , vol.95 , pp. 1606-1611
    • Diller, L1    Sexsmith, E2    Gottlieb, A3    Li, FP4    Malkin, D5
  • 47
    • 0027405940 scopus 로고
    • Screening for germ line p53 mutations in children with malignant tumors and a family history of cancer
    • L Brugieres M Gardes C Moutou A Chompret V Maresse A Martin Screening for germ line p53 mutations in children with malignant tumors and a family history of cancer Cancer Res 53 1993 452 455
    • (1993) Cancer Res , vol.53 , pp. 452-455
    • Brugieres, L1    Gardes, M2    Moutou, C3    Chompret, A4    Maresse, V5    Martin, A6
  • 48
    • 0026577713 scopus 로고
    • Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemia
    • CA Felix MM Nau T Takahashi T Mitsudomi I Chiba DG Poplack Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemia J Clin Invest 89 1992 640 647
    • (1992) J Clin Invest , vol.89 , pp. 640-647
    • Felix, CA1    Nau, MM2    Takahashi, T3    Mitsudomi, T4    Chiba, I5    Poplack, DG6
  • 49
    • 0028566388 scopus 로고
    • A de novo p53 germline mutation affecting codon 151 in a six year old child with multiple tumors
    • MI Gutierrez KG Bathia C Barreiro G Spangler E Schvartzmann F Sackmann A de novo p53 germline mutation affecting codon 151 in a six year old child with multiple tumors Hum Mol Genet 3 1994 2247 2248
    • (1994) Hum Mol Genet , vol.3 , pp. 2247-2248
    • Gutierrez, MI1    Bathia, KG2    Barreiro, C3    Spangler, G4    Schvartzmann, E5    Sackmann, F6
  • 52
    • 0026530299 scopus 로고
    • Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms
    • D Malkin KW Jolly N Barbier AT Look SH Friend MC Gebhardt Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms N Engl J Med 326 1992 1309 1315
    • (1992) N Engl J Med , vol.326 , pp. 1309-1315
    • Malkin, D1    Jolly, KW2    Barbier, N3    Look, AT4    Friend, SH5    Gebhardt, MC6
  • 53
    • 0030017174 scopus 로고    scopus 로고
    • Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-21
    • N Rahman L Arbour P Tonin J Renshaw J Pelletier S Baruchel Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-21 Nat Genet 13 1996 461 463
    • (1996) Nat Genet , vol.13 , pp. 461-463
    • Rahman, N1    Arbour, L2    Tonin, P3    Renshaw, J4    Pelletier, J5    Baruchel, S6
  • 54
    • 0028059816 scopus 로고
    • Genetic events in the development of Wilms' tumor
    • MJ Coppes DA Haber PE Grundy Genetic events in the development of Wilms' tumor N Engl J Med 331 1994 586 590
    • (1994) N Engl J Med , vol.331 , pp. 586-590
    • Coppes, MJ1    Haber, DA2    Grundy, PE3
  • 55
    • 0025099787 scopus 로고
    • Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
    • K Call T Glaser C Ito A Buckler J Pelletier D Haber Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus Cell 60 1990 509 520
    • (1990) Cell , vol.60 , pp. 509-520
    • Call, K1    Glaser, T2    Ito, C3    Buckler, A4    Pelletier, J5    Haber, D6
  • 56
    • 0025098654 scopus 로고
    • Homozygous deletion in Wilms tumors of a zinc finger gene identified by chromosome jumping
    • M Gessler A Poutska W Cavanee RL Neve SH Orkin GAP Bruns Homozygous deletion in Wilms tumors of a zinc finger gene identified by chromosome jumping Nature 343 1990 774 778
    • (1990) Nature , vol.343 , pp. 774-778
    • Gessler, M1    Poutska, A2    Cavanee, W3    Neve, RL4    Orkin, SH5    Bruns, GAP6
  • 57
    • 0025288793 scopus 로고
    • An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor
    • D Haber A Buckler T Glaser K Call J Pelletier R Sohn An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor Cell 61 1990 1257 1269
    • (1990) Cell , vol.61 , pp. 1257-1269
    • Haber, D1    Buckler, A2    Glaser, T3    Call, K4    Pelletier, J5    Sohn, R6
  • 60
    • 0026094584 scopus 로고
    • Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
    • J Pelletier W Bruening CE Kashtan SM Mauer JC Manivel JE Striegel Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome Cell 67 1991 437 447
    • (1991) Cell , vol.67 , pp. 437-447
    • Pelletier, J1    Bruening, W2    Kashtan, CE3    Mauer, SM4    Manivel, JC5    Striegel, JE6
  • 62
    • 0027771747 scopus 로고
    • WT1-mediated growth suppression of Wilms tumor cells expressing a WT1 splicing variant
    • D Haber S Park S Maheswaran C Englert G Re D Hazen-Marton WT1-mediated growth suppression of Wilms tumor cells expressing a WT1 splicing variant Science 262 1993 2057 2059
    • (1993) Science , vol.262 , pp. 2057-2059
    • Haber, D1    Park, S2    Maheswaran, S3    Englert, C4    Re, G5    Hazen-Marton, D6
  • 63
    • 0025788974 scopus 로고
    • WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumor
    • J Pelletier W Bruening FP Li DA Haber T Glaser DE Housman WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumor Nature 353 1991 431 434
    • (1991) Nature , vol.353 , pp. 431-434
    • Pelletier, J1    Bruening, W2    Li, FP3    Haber, DA4    Glaser, T5    Housman, DE6
  • 64
    • 0027228366 scopus 로고
    • Mutational screening of the Wilms's tumor gene, WT1, in males with genital abnormalities
    • PA Clarkson HR Davies DM Williams R Chaudhary IA Hughes MN Patterson Mutational screening of the Wilms's tumor gene, WT1, in males with genital abnormalities J Med Genet 30 1993 767 772
    • (1993) J Med Genet , vol.30 , pp. 767-772
    • Clarkson, PA1    Davies, HR2    Williams, DM3    Chaudhary, R4    Hughes, IA5    Patterson, MN6
  • 66
    • 0025569330 scopus 로고
    • The contribution of inherited predisposition to cancer incidence
    • D Easton J Peto The contribution of inherited predisposition to cancer incidence Cancer Surv 9 1990 395 415
    • (1990) Cancer Surv , vol.9 , pp. 395-415
    • Easton, D1    Peto, J2
  • 67
    • 0029086057 scopus 로고
    • Screening for cancer in high risk families
    • SA Narod Screening for cancer in high risk families Clin Biochem 23 1995 367 372
    • (1995) Clin Biochem , vol.23 , pp. 367-372
    • Narod, SA1
  • 69
    • 0030074994 scopus 로고    scopus 로고
    • Emotional and behavioral responses to genetic testing for susceptibility to cancer
    • C Lermen RT Croyle Emotional and behavioral responses to genetic testing for susceptibility to cancer Oncology 10 1996 191 199
    • (1996) Oncology , vol.10 , pp. 191-199
    • Lermen, C1    Croyle, RT2
  • 70
    • 0029683018 scopus 로고    scopus 로고
    • Genetic testing and counseling in familial adenomatous polyposis
    • G Petersen JD Brensiger Genetic testing and counseling in familial adenomatous polyposis Oncology 10 1996 89 164
    • (1996) Oncology , vol.10 , pp. 89-164
    • Petersen, G1    Brensiger, JD2
  • 71
    • 0029446633 scopus 로고
    • Gene tests and counselling for colorectal cancer risk: lessons from familial polyposis
    • G Petersen P Boyd Gene tests and counselling for colorectal cancer risk: lessons from familial polyposis Natl Cancer Inst Monogr 17 1995 67 71
    • (1995) Natl Cancer Inst Monogr , vol.17 , pp. 67-71
    • Petersen, G1    Boyd, P2
  • 72
    • 0030019446 scopus 로고    scopus 로고
    • Attitudes of 47 mothers of pediatric oncology patients toward genetic testing for cancer predisposition
    • A Patenaude L Basili D Fairclough F Li Attitudes of 47 mothers of pediatric oncology patients toward genetic testing for cancer predisposition J Clin Oncol 14 1996 415 421
    • (1996) J Clin Oncol , vol.14 , pp. 415-421
    • Patenaude, A1    Basili, L2    Fairclough, D3    Li, F4
  • 73
    • 0029999046 scopus 로고
    • Parents' responses to predictive genetic testing in their children: report of a single case study
    • S Michie V McDonald M Bobrow C McKeown T Marteau Parents' responses to predictive genetic testing in their children: report of a single case study J Med Genet 33 1995 313 318
    • (1995) J Med Genet , vol.33 , pp. 313-318
    • Michie, S1    McDonald, V2    Bobrow, M3    McKeown, C4    Marteau, T5
  • 74
    • 0027482439 scopus 로고
    • Privacy rules for DNA databanks
    • GJ Annas Privacy rules for DNA databanks JAMA 270 1993 2346 2350
    • (1993) JAMA , vol.270 , pp. 2346-2350
    • Annas, GJ1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.