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Volumn 5, Issue , 2004, Pages 1-14

Genetic testing in primary care

Author keywords

Family history; Gene variant; Mutation; Prevention; Risk

Indexed keywords

DECISION MAKING; FAMILY HISTORY; GENETIC ANALYSIS; GENETIC RISK; HUMAN; MASS SCREENING; POLICY; PRACTICE GUIDELINE; PRIMARY MEDICAL CARE; REVIEW; RISK ASSESSMENT; SYMPTOMATOLOGY;

EID: 5444262324     PISSN: 15278204     EISSN: None     Source Type: Book Series    
DOI: 10.1146/annurev.genom.5.061903.180029     Document Type: Review
Times cited : (62)

References (78)
  • 1
    • 0035349420 scopus 로고    scopus 로고
    • Clinical management guidelines for obstetricians-gynecologists. Prenatal diagnosis of fetal chromosome abnormalities
    • Am. Coll. Obstet. Gynecol. Comm. Pr. Bull. ACOG Pr. Bull. 2001. Clinical management guidelines for obstetricians-gynecologists. Prenatal diagnosis of fetal chromosome abnormalities. Obstet. Gynecol. 97(Suppl.):1-12
    • (2001) Obstet. Gynecol. , vol.97 , Issue.SUPPL. , pp. 1-12
  • 2
    • 0038501057 scopus 로고    scopus 로고
    • American Society of Clinical Oncology policy statement update: Genetic testing for cancer susceptibility
    • Am. Soc. Clin. Oncol. 2003. American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility. J. Clin. Oncol. 21:2397-406
    • (2003) J. Clin. Oncol. , vol.21 , pp. 2397-2406
  • 3
    • 0016822465 scopus 로고
    • Genetic counseling
    • Am. Soc. Human Genetics. 1975. Genetic counseling. Am. J. Hum. Genet. 27:240-42
    • (1975) Am. J. Hum. Genet. , vol.27 , pp. 240-242
  • 4
    • 0038744296 scopus 로고    scopus 로고
    • Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysis of 22 studies
    • Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, et al. 2003. Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies. Am. J. Hum. Genet. 72:1117-30
    • (2003) Am. J. Hum. Genet. , vol.72 , pp. 1117-1130
    • Antoniou, A.1    Pharoah, P.D.2    Narod, S.3    Risch, H.A.4    Eyfjord, J.E.5
  • 7
    • 0037151382 scopus 로고    scopus 로고
    • On the use of familial aggregation in population-based case probands for calculating penetrance
    • Begg C. 2002. On the use of familial aggregation in population-based case probands for calculating penetrance. J. Natl. Cancer Inst. 94:1221-26
    • (2002) J. Natl. Cancer Inst. , vol.94 , pp. 1221-1226
    • Begg, C.1
  • 8
    • 0036899479 scopus 로고    scopus 로고
    • Internet-based risk assessment and decision support for the management of familial cancer in primary care: A survey of GPs' attitudes and intentions
    • Braithwaite D, Sutton S, Smithson WH, Emery J. 2002. Internet-based risk assessment and decision support for the management of familial cancer in primary care: a survey of GPs' attitudes and intentions. Fam. Pract. 19:587-90
    • (2002) Fam. Pract. , vol.19 , pp. 587-590
    • Braithwaite, D.1    Sutton, S.2    Smithson, W.H.3    Emery, J.4
  • 10
    • 0032496881 scopus 로고    scopus 로고
    • Hereditary hemochromatosis: Gene discovery and its implications for population-based screening
    • Burke W, Thomson E, Khoury MJ, McDonnell SM, Press N, et al. 1998. Hereditary hemochromatosis: gene discovery and its implications for population-based screening. JAMA 280:172-78
    • (1998) JAMA , vol.280 , pp. 172-178
    • Burke, W.1    Thomson, E.2    Khoury, M.J.3    McDonnell, S.M.4    Press, N.5
  • 11
    • 0034770853 scopus 로고    scopus 로고
    • Categorizing genetic tests to identify their ethical, legal and social implications
    • Burke W, Pinsky L, Press N. 2001. Categorizing genetic tests to identify their ethical, legal and social implications. Am. J. Med. Genet. (Semin. Med Genet.) 106:233-40
    • (2001) Am. J. Med. Genet. (Semin. Med Genet.) , vol.106 , pp. 233-240
    • Burke, W.1    Pinsky, L.2    Press, N.3
  • 12
    • 84866587917 scopus 로고    scopus 로고
    • Hereditary haemochromatosis: A realistic approach to prevention of iron overload disease in the population
    • Burke W, Reyes M, Imperatore G. 2002. Hereditary haemochromatosis: a realistic approach to prevention of iron overload disease in the population. Best. Pract. Res. Clin. Haematol. 15:315-28
    • (2002) Best. Pract. Res. Clin. Haematol. , vol.15 , pp. 315-328
    • Burke, W.1    Reyes, M.2    Imperatore, G.3
  • 15
    • 0001539758 scopus 로고    scopus 로고
    • What should the law say about disclosure of genetic information to relatives?
    • Clayton EW. 1998. What should the law say about disclosure of genetic information to relatives? J. Health Care Law Policy 1:373-90
    • (1998) J. Health Care Law Policy , vol.1 , pp. 373-390
    • Clayton, E.W.1
  • 16
    • 0030846219 scopus 로고    scopus 로고
    • Preparing health professionals for the genetic revolution
    • Collins FS. 1997. Preparing health professionals for the genetic revolution. JAMA 278:1285-86
    • (1997) JAMA , vol.278 , pp. 1285-1286
    • Collins, F.S.1
  • 17
    • 0033168459 scopus 로고    scopus 로고
    • Shattuck lecture: Medical and societal consequences of the Human Genome Project
    • Collins FS. 1999. Shattuck lecture: medical and societal consequences of the Human Genome Project. N. Engl. J. Med. 341:28-37
    • (1999) N. Engl. J. Med. , vol.341 , pp. 28-37
    • Collins, F.S.1
  • 18
    • 0033214004 scopus 로고    scopus 로고
    • Screening for factor V Leiden mutation before prescribing combination oral contraceptives
    • Creinen MD, Lisman R, Strickler RC. 1999. Screening for factor V Leiden mutation before prescribing combination oral contraceptives. Fertil. Steril. 72:646-51
    • (1999) Fertil. Steril. , vol.72 , pp. 646-651
    • Creinen, M.D.1    Lisman, R.2    Strickler, R.C.3
  • 20
    • 0035746390 scopus 로고    scopus 로고
    • The 22q11.2 deletion: From diversity to a single gene theory
    • DeDecker HP, Lawrenson JB. 2001. The 22q11.2 deletion: from diversity to a single gene theory. Genet. Med. 3:2-5
    • (2001) Genet. Med. , vol.3 , pp. 2-5
    • DeDecker, H.P.1    Lawrenson, J.B.2
  • 21
    • 0034994092 scopus 로고    scopus 로고
    • The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation
    • De Stefano V, Martinelli I, Mannucci PM, Paciaroni K, Rossi E, et al. 2001. The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation. Br. J. Haematol. 113:630-35
    • (2001) Br. J. Haematol. , vol.113 , pp. 630-635
    • De Stefano, V.1    Martinelli, I.2    Mannucci, P.M.3    Paciaroni, K.4    Rossi, E.5
  • 22
    • 0242676045 scopus 로고    scopus 로고
    • The importance of screening for hemochromatosis
    • Dubois S, Kowdley K. 2003. The importance of screening for hemochromatosis. Arch. Intern. Med. 163:2424-25
    • (2003) Arch. Intern. Med. , vol.163 , pp. 2424-2425
    • Dubois, S.1    Kowdley, K.2
  • 23
    • 0034840147 scopus 로고    scopus 로고
    • Combined effect of factor V Leiden and prothroimbin 20210A on the risk of venous thromboembolism - Pooled analysis of 8 case-control studies including 2310 cases and 3204 controls
    • Study group for pooled-analysis in venous thromboembolism
    • Emmerich J, Rosendaal F, Cattaneo M, Margaglione M, De Stefano V, Cumming T. 2001. Combined effect of factor V Leiden and prothroimbin 20210A on the risk of venous thromboembolism - pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study group for pooled-analysis in venous thromboembolism. Thromb. Haemostat. 86:809-16
    • (2001) Thromb. Haemostat. , vol.86 , pp. 809-816
    • Emmerich, J.1    Rosendaal, F.2    Cattaneo, M.3    Margaglione, M.4    De Stefano, V.5    Cumming, T.6
  • 24
    • 0035962372 scopus 로고    scopus 로고
    • The complexities of predictive genetic testing
    • Evans JP, Skrzynia C, Burke W. 2001. The complexities of predictive genetic testing. Br. Med. J. 322:1052-56
    • (2001) Br. Med. J. , vol.322 , pp. 1052-1056
    • Evans, J.P.1    Skrzynia, C.2    Burke, W.3
  • 26
    • 0030901262 scopus 로고    scopus 로고
    • The use and interpretation of commercial APC gene testing for familial adenomatous polyposis
    • Giardiello FM, Brensinger JD, Petersen GM, Luce MC, Hylind LM, et al. 1997. The use and interpretation of commercial APC gene testing for familial adenomatous polyposis. N. Engl. J. Med. 336:823-27
    • (1997) N. Engl. J. Med. , vol.336 , pp. 823-827
    • Giardiello, F.M.1    Brensinger, J.D.2    Petersen, G.M.3    Luce, M.C.4    Hylind, L.M.5
  • 27
    • 0032503684 scopus 로고    scopus 로고
    • Profile of preparticipation cardiovascular screening for high school athletes
    • Glover DW, Maron BJ. 1998. Profile of preparticipation cardiovascular screening for high school athletes. JAMA 279:1817-19
    • (1998) JAMA , vol.279 , pp. 1817-1819
    • Glover, D.W.1    Maron, B.J.2
  • 28
    • 0037048668 scopus 로고    scopus 로고
    • Limitations of direct-to-consumer advertising for clinical genetic testing
    • Gollust SE, Hull SC, Wilfond BS. 2002. Limitations of direct-to-consumer advertising for clinical genetic testing. JAMA 288(14):1762-67
    • (2002) JAMA , vol.288 , Issue.14 , pp. 1762-1767
    • Gollust, S.E.1    Hull, S.C.2    Wilfond, B.S.3
  • 30
    • 0033005138 scopus 로고    scopus 로고
    • National confidential enquiry into counselling for genetic disorders by non-geneticists: General recommendations and specific standards for improving care
    • Harris R, Lane B, Harris H, Williamson P, Dodge J, et al. 1999. National confidential enquiry into counselling for genetic disorders by non-geneticists: general recommendations and specific standards for improving care. Br. J. Obstet. Gynaecol. 106:658-63
    • (1999) Br. J. Obstet. Gynaecol. , vol.106 , pp. 658-663
    • Harris, R.1    Lane, B.2    Harris, H.3    Williamson, P.4    Dodge, J.5
  • 31
    • 0036565886 scopus 로고    scopus 로고
    • How we diagnose and treat deep venous thrombosis
    • Hirsh J, Lee AY. 2002. How we diagnose and treat deep venous thrombosis. Blood 99:3102-10
    • (2002) Blood , vol.99 , pp. 3102-3110
    • Hirsh, J.1    Lee, A.Y.2
  • 34
    • 0034434840 scopus 로고    scopus 로고
    • Population-based genetic screening for reproductive counseling: The Tay-Sachs disease model
    • Kaback MM. 2000. Population-based genetic screening for reproductive counseling: the Tay-Sachs disease model. Eur. J. Pediatr. 159(Suppl. 2):S192-95
    • (2000) Eur. J. Pediatr. , vol.159 , Issue.SUPPL. 2
    • Kaback, M.M.1
  • 35
    • 0034611908 scopus 로고    scopus 로고
    • Genetic epidemiology
    • Kaprio J. 2000. Genetic epidemiology. Br. Med. J. 320:1257-59
    • (2000) Br. Med. J. , vol.320 , pp. 1257-1259
    • Kaprio, J.1
  • 38
    • 0029831202 scopus 로고    scopus 로고
    • Genetic discrimination: Perspectives of consumers
    • Lapham EV, Kozma C, Weiss JO. 1996. Genetic discrimination: perspectives of consumers. Science 274:621-24
    • (1996) Science , vol.274 , pp. 621-624
    • Lapham, E.V.1    Kozma, C.2    Weiss, J.O.3
  • 39
    • 0032512261 scopus 로고    scopus 로고
    • Genetic discrimination in life insurance: Empirical evidence from a cross-sectional survey of genetic support groups in the Untied Kingdom
    • Low L, King S, Wilkie T. 1998. Genetic discrimination in life insurance: empirical evidence from a cross-sectional survey of genetic support groups in the Untied Kingdom. Br. Med. J. 317:1632-35
    • (1998) Br. Med. J. , vol.317 , pp. 1632-1635
    • Low, L.1    King, S.2    Wilkie, T.3
  • 40
    • 0035962376 scopus 로고    scopus 로고
    • Genetic risk and behavioural change
    • Marteau TM, Lerman C. 2001. Genetic risk and behavioural change. Br. Med. J. 322:1056-59
    • (2001) Br. Med. J. , vol.322 , pp. 1056-1059
    • Marteau, T.M.1    Lerman, C.2
  • 41
    • 0034487766 scopus 로고    scopus 로고
    • The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both
    • Martinelli I, Bucciarelli P, Margaglione M, De Stefano V, Castaman G, Mannucci PM. 2000. The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both. Br. J. Haematol. 111:1223-29
    • (2000) Br. J. Haematol. , vol.111 , pp. 1223-1229
    • Martinelli, I.1    Bucciarelli, P.2    Margaglione, M.3    De Stefano, V.4    Castaman, G.5    Mannucci, P.M.6
  • 43
    • 0035746391 scopus 로고    scopus 로고
    • Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: Cast a wide FISHing net!
    • McDonald-McGinn DM, Tonnesen MK, Laufer-Cahana A, Finucane B, Driscoll DA, et al. 2001. Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net! Genet. Med. 3:23-29
    • (2001) Genet. Med. , vol.3 , pp. 23-29
    • McDonald-McGinn, D.M.1    Tonnesen, M.K.2    Laufer-Cahana, A.3    Finucane, B.4    Driscoll, D.A.5
  • 44
    • 10744223296 scopus 로고    scopus 로고
    • Hereditary hemochromatosis and its elusive natural history
    • McDonnell SM, Parrish RG. 2003. Hereditary hemochromatosis and its elusive natural history. Arch. Intern. Med. 163:2421-23
    • (2003) Arch. Intern. Med. , vol.163 , pp. 2421-2423
    • McDonnell, S.M.1    Parrish, R.G.2
  • 45
    • 0034034158 scopus 로고    scopus 로고
    • Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia
    • McLeod HL, Krynetski EY, Relling MV, Evans WE. 2000. Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia. Leukemia 14:567-72
    • (2000) Leukemia , vol.14 , pp. 567-572
    • McLeod, H.L.1    Krynetski, E.Y.2    Relling, M.V.3    Evans, W.E.4
  • 46
    • 0031718588 scopus 로고    scopus 로고
    • Clinical implications of cystic fibrosis transmembrane conductance regulator mutations
    • Mickle JE, Cutting GR. 1998. Clinical implications of cystic fibrosis transmembrane conductance regulator mutations. Clin. Chest Med. 19:443-58
    • (1998) Clin. Chest Med. , vol.19 , pp. 443-458
    • Mickle, J.E.1    Cutting, G.R.2
  • 47
    • 0035806996 scopus 로고    scopus 로고
    • A prospective study of asymptomatic carriers of the factor V Leiden mutation to determine the incidence of venous thromboembolism
    • Middeldorp S, Meinardi JR, Koopman MM, van Pampus EC, Hamulyak K, et al. 2001. A prospective study of asymptomatic carriers of the factor V Leiden mutation to determine the incidence of venous thromboembolism. Ann. Intern. Med. 135:322-27
    • (2001) Ann. Intern. Med. , vol.135 , pp. 322-327
    • Middeldorp, S.1    Meinardi, J.R.2    Koopman, M.M.3    Van Pampus, E.C.4    Hamulyak, K.5
  • 48
    • 10744231817 scopus 로고    scopus 로고
    • Guidelines for breast and ovarian cancer genetic counseling referral: Adoption and implementation in HMOs
    • Mouchawar J, Valentine Goins K, Somkin C, Puleo E, Hensley Alford S, et al. 2003. Guidelines for breast and ovarian cancer genetic counseling referral: adoption and implementation in HMOs. Genet. Med. 5:444-50
    • (2003) Genet. Med. , vol.5 , pp. 444-450
    • Mouchawar, J.1    Valentine Goins, K.2    Somkin, C.3    Puleo, E.4    Hensley Alford, S.5
  • 49
    • 0027243348 scopus 로고
    • Summary of the second report of the expert panel
    • Natl. Cholest. Educ. Progr. (NCEP) Expert Panel Detect., Eval. Treat. High Cholest. Adults (Adult Treat. Panel II). 1993. Summary of the second report of the expert panel. JAMA 269:3015-23
    • (1993) JAMA , vol.269 , pp. 3015-3023
  • 50
    • 5444266347 scopus 로고    scopus 로고
    • Pate v. Threlkel. 1995. 661 So.2d 278 Florida
    • Pate v. Threlkel. 1995. 661 So.2d 278 Florida
  • 51
    • 0035962320 scopus 로고    scopus 로고
    • Online medical genetics resources: A U.S. perspective
    • Pagon RA, Pinsky L, Beahler C. 2001. Online medical genetics resources: a U.S. perspective. Br. Med. J. 322:1035-38
    • (2001) Br. Med. J. , vol.322 , pp. 1035-1038
    • Pagon, R.A.1    Pinsky, L.2    Beahler, C.3
  • 54
    • 0042806076 scopus 로고    scopus 로고
    • Role of the geneticist in testing and counseling for inherited thrombophilia
    • Reich LM, Bower M, Key NS. 2003. Role of the geneticist in testing and counseling for inherited thrombophilia. Genet. Med. 5:133-43
    • (2003) Genet. Med. , vol.5 , pp. 133-143
    • Reich, L.M.1    Bower, M.2    Key, N.S.3
  • 56
    • 0037431013 scopus 로고    scopus 로고
    • Long-term, low-intensity warfarin therapy for the prevention of recurrent venous thromboembolism
    • Ridker PM, Goldhaber SZ, Danielson E, Rosenberg Y, Eby CS, et al. 2003. Long-term, low-intensity warfarin therapy for the prevention of recurrent venous thromboembolism. N. Engl. J. Med. 348:1425-34
    • (2003) N. Engl. J. Med. , vol.348 , pp. 1425-1434
    • Ridker, P.M.1    Goldhaber, S.Z.2    Danielson, E.3    Rosenberg, Y.4    Eby, C.S.5
  • 57
    • 0033519051 scopus 로고
    • Venous thrombosis: A multicausal disease
    • Rosendal F. 1993. Venous thrombosis: a multicausal disease. Lancet 353:1167-73
    • (1993) Lancet , vol.353 , pp. 1167-1173
    • Rosendal, F.1
  • 58
    • 0034772316 scopus 로고    scopus 로고
    • Referral of patients with a family history of breast/ovarian cancer-GPs' knowledge and expectations
    • Rose PW, Watson E, Yudkin P, Emery J, Murphy M, et al. 2001. Referral of patients with a family history of breast/ovarian cancer-GPs' knowledge and expectations. Fam. Pract. 18:487-90
    • (2001) Fam. Pract. , vol.18 , pp. 487-490
    • Rose, P.W.1    Watson, E.2    Yudkin, P.3    Emery, J.4    Murphy, M.5
  • 59
    • 5444229184 scopus 로고    scopus 로고
    • Safer v. Pack. 1996. 677 A. 2d 1188 NJ
    • Safer v. Pack. 1996. 677 A. 2d 1188 NJ
  • 60
    • 0036123913 scopus 로고    scopus 로고
    • Family history and colorectal cancer screening: A survey of physician knowledge and practice patterns
    • Schroy PC 3rd, Barrison AF, Ling BS, Wilson S, Geller AC. 2002. Family history and colorectal cancer screening: a survey of physician knowledge and practice patterns. Am. J. Gastroenterol. 97:1031-36
    • (2002) Am. J. Gastroenterol. , vol.97 , pp. 1031-1036
    • Schroy III, P.C.1    Barrison, A.F.2    Ling, B.S.3    Wilson, S.4    Geller, A.C.5
  • 61
    • 0033452167 scopus 로고    scopus 로고
    • Genetic susceptibility for specific cancers: Medical liability of the clinician
    • Severin MJ. 1999. Genetic susceptibility for specific cancers: medical liability of the clinician. Cancer 86:2564-69
    • (1999) Cancer , vol.86 , pp. 2564-2569
    • Severin, M.J.1
  • 63
    • 0028778750 scopus 로고
    • Is primary care essential?
    • Starfield B. 1994. Is primary care essential? Lancet. 344:1129-33
    • (1994) Lancet , vol.344 , pp. 1129-1133
    • Starfield, B.1
  • 64
    • 0035962314 scopus 로고    scopus 로고
    • Online medical genetics resources: A U.K. perspective
    • Stewart A, Haites N, Rose P. 2001. Online medical genetics resources: a U.K. perspective. Br. Med. J. 322:1037-39
    • (2001) Br. Med. J. , vol.322 , pp. 1037-1039
    • Stewart, A.1    Haites, N.2    Rose, P.3
  • 65
    • 0032749260 scopus 로고    scopus 로고
    • Are general practitioners willing and able to provide genetic services for common diseases
    • Suchard MA, Yudkin P, Sinheimer JS. 1999. Are general practitioners willing and able to provide genetic services for common diseases. J. Genet. Couns. 8:301-11
    • (1999) J. Genet. Couns. , vol.8 , pp. 301-311
    • Suchard, M.A.1    Yudkin, P.2    Sinheimer, J.S.3
  • 66
    • 0042905739 scopus 로고    scopus 로고
    • Barriers to the provision of genetic services by primary care physicians: A systematic review of the literature
    • Suther S, Goodson P. 2003. Barriers to the provision of genetic services by primary care physicians: a systematic review of the literature. Genet. Med. 5:70-76
    • (2003) Genet. Med. , vol.5 , pp. 70-76
    • Suther, S.1    Goodson, P.2
  • 67
    • 0037080326 scopus 로고    scopus 로고
    • Identification and referral of families at high risk for cancer susceptibility
    • Sweet KM, Bradley TL, Westman JA. 2002. Identification and referral of families at high risk for cancer susceptibility. J. Clin. Oncol. 20:528-37
    • (2002) J. Clin. Oncol. , vol.20 , pp. 528-537
    • Sweet, K.M.1    Bradley, T.L.2    Westman, J.A.3
  • 68
    • 0001373172 scopus 로고    scopus 로고
    • Newborn screening: A blueprint for the future - A call for a national agenda on state newborn screening programs
    • Task Force Newborn Screening. 2000. Newborn screening: a blueprint for the future - a call for a national agenda on state newborn screening programs. Pediatrics 106:389-422
    • (2000) Pediatrics , vol.106 , pp. 389-422
  • 70
    • 0034787337 scopus 로고    scopus 로고
    • Evaluation of the impact of two educational interventions on GP management of familial breast/ovarian cancer cases: A cluster randomized controlled trial
    • Watson E, Clements A, Yudkin P, Rose P, Bukach C, et al. 2001. Evaluation of the impact of two educational interventions on GP management of familial breast/ovarian cancer cases: a cluster randomized controlled trial. Br. J. Gen. Pract. 51:817-21
    • (2001) Br. J. Gen. Pract. , vol.51 , pp. 817-821
    • Watson, E.1    Clements, A.2    Yudkin, P.3    Rose, P.4    Bukach, C.5
  • 71
    • 0032483689 scopus 로고    scopus 로고
    • Uncertainties in genetic testing for chronic disease
    • Welch HG, Burke W 1998. Uncertainties in genetic testing for chronic disease. JAMA 280:1525-27
    • (1998) JAMA , vol.280 , pp. 1525-1527
    • Welch, H.G.1    Burke, W.2
  • 72
    • 0037421584 scopus 로고    scopus 로고
    • Inheritance and drug response
    • Weinshilboum R. 2003. Inheritance and drug response. N. Engl. J. Med. 348:529-37
    • (2003) N. Engl. J. Med. , vol.348 , pp. 529-537
    • Weinshilboum, R.1
  • 73
    • 5444231578 scopus 로고    scopus 로고
    • Multiple endocrine neoplasia type 2
    • Weisner G, Snow K. 2003. Multiple endocrine neoplasia type 2. Gene Rev. http://www.genetests.org
    • (2003) Gene Rev.
    • Weisner, G.1    Snow, K.2
  • 74
    • 0034478002 scopus 로고    scopus 로고
    • Preimplantation genetic diagnosis: Applications for molecular medicine
    • Wells D, Delhanty JD. 2001. Preimplantation genetic diagnosis: applications for molecular medicine. Trends Mol. Med. 7:23-30
    • (2001) Trends Mol. Med. , vol.7 , pp. 23-30
    • Wells, D.1    Delhanty, J.D.2
  • 76
    • 84986560856 scopus 로고    scopus 로고
    • Applying genetic strategies to prevent atherosclerosis
    • ed. MJ Khoury, W Burke, E Thomson. New York: Oxford Univ. Press
    • Williams RR, Hopkins PN, Wu LL, Hunt SC. 2000. Applying genetic strategies to prevent atherosclerosis. In Genetics and Public Health, ed. MJ Khoury, W Burke, E Thomson, pp. 463-85. New York: Oxford Univ. Press
    • (2000) Genetics and Public Health , pp. 463-485
    • Williams, R.R.1    Hopkins, P.N.2    Wu, L.L.3    Hunt, S.C.4
  • 77
    • 0037310758 scopus 로고    scopus 로고
    • Colorectal cancer screening and surveillance: Clinical guidelines and rationale-update based on new evidence
    • Winawer S, Reicher R, Rex D, Bond J, Burt R, et al. 2003. Colorectal cancer screening and surveillance: clinical guidelines and rationale-update based on new evidence. Gastroenterology 124:544-60
    • (2003) Gastroenterology , vol.124 , pp. 544-560
    • Winawer, S.1    Reicher, R.2    Rex, D.3    Bond, J.4    Burt, R.5


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