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Volumn 39, Issue 4, 1996, Pages 873-884

Standards of care and ethical concerns in genetic testing and screening

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA FETOPROTEIN;

EID: 0029803867     PISSN: 00099201     EISSN: None     Source Type: Journal    
DOI: 10.1097/00003081-199612000-00014     Document Type: Review
Times cited : (8)

References (41)
  • 1
    • 0026840247 scopus 로고
    • Torts and the double helix: Malpractice liability for failure to warn of genetic risks
    • Andrews LB. Torts and the double helix: Malpractice liability for failure to warn of genetic risks. Houston Law Review. 1992;29:149-184.
    • (1992) Houston Law Review , vol.29 , pp. 149-184
    • Andrews, L.B.1
  • 2
    • 0028783773 scopus 로고
    • Aberrant subcellular localization of BRCA1 in breast cancer
    • Chen Y, Chen CF, Riley DJ, et al. Aberrant subcellular localization of BRCA1 in breast cancer. Science. 1995;270:789-91.
    • (1995) Science , vol.270 , pp. 789-791
    • Chen, Y.1    Chen, C.F.2    Riley, D.J.3
  • 4
    • 0029083814 scopus 로고
    • The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals
    • Struewing J, Abeliovich D, Peretz T, et al. The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals. Nature Genet. 1995;11:198-200.
    • (1995) Nature Genet , vol.11 , pp. 198-200
    • Struewing, J.1    Abeliovich, D.2    Peretz, T.3
  • 5
    • 0027499439 scopus 로고
    • Altered fates - Counseling families with inherited breast cancer
    • Breo DL. Altered fates - Counseling families with inherited breast cancer. JAMA. 1993;269:2017-2022, 2017.
    • (1993) JAMA , vol.269 , pp. 2017-2022
    • Breo, D.L.1
  • 6
    • 0028814530 scopus 로고
    • Assessment and counseling for women with a family history of breast cancer
    • Hoskins KF, Stopfer JE. Assessment and counseling for women with a family history of breast cancer. JAMA. 1995;273:577-585.
    • (1995) JAMA , vol.273 , pp. 577-585
    • Hoskins, K.F.1    Stopfer, J.E.2
  • 7
    • 23444445336 scopus 로고
    • Statement on use of DNA testing for presymptomatic identification of cancer risk
    • National Advisory Council for Human Genome Research. Statement on use of DNA testing for presymptomatic identification of cancer risk. JAMA. 1994;271:785.
    • (1994) JAMA , vol.271 , pp. 785
  • 8
    • 0028148836 scopus 로고
    • Statement of the American Society of Human Genetics on genetic testing for breast and ovarian cancer predisposition
    • American Society of Human Genetics. Statement of the American Society of Human Genetics on genetic testing for breast and ovarian cancer predisposition. Am J Hum Genet. 1994;55:i- iv.
    • (1994) Am J Hum Genet , vol.55
  • 9
    • 0030049353 scopus 로고    scopus 로고
    • BRCA1 - Lots of mutations, lots of dilemmas
    • Collins FS. BRCA1 - Lots of mutations, lots of dilemmas. N Engl J Med. 1996;334:186-188.
    • (1996) N Engl J Med , vol.334 , pp. 186-188
    • Collins, F.S.1
  • 10
    • 0028761242 scopus 로고
    • Generic consent for genetic screening
    • Elias S, Annas GJ. Generic consent for genetic screening. N Engl J Med. 1994;330:1611-1613.
    • (1994) N Engl J Med , vol.330 , pp. 1611-1613
    • Elias, S.1    Annas, G.J.2
  • 11
    • 0025307621 scopus 로고
    • Genetics, ethics, and audit
    • Clarke A. Genetics, ethics, and audit. Lancet. 1990;335:1145-1147.
    • (1990) Lancet , vol.335 , pp. 1145-1147
    • Clarke, A.1
  • 12
    • 0026295052 scopus 로고
    • Screening for Tay-Sachs disease: A note of caution
    • Rosner F. Screening for Tay-Sachs disease: A note of caution. J Clin Ethics. 1991;2:251-252.
    • (1991) J Clin Ethics , vol.2 , pp. 251-252
    • Rosner, F.1
  • 13
    • 0025998982 scopus 로고
    • Is non-directive genetic counselling possible?
    • Clarke A. Is non-directive genetic counselling possible? Lancet. 1991;338:998-1001.
    • (1991) Lancet , vol.338 , pp. 998-1001
    • Clarke, A.1
  • 14
    • 0028353474 scopus 로고
    • Psychological issues in genetic testing for breast cancer susceptibility
    • Lerman C, Croyle R. Psychological issues in genetic testing for breast cancer susceptibility. Arch Internal Med. 1994;154:609-616.
    • (1994) Arch Internal Med , vol.154 , pp. 609-616
    • Lerman, C.1    Croyle, R.2
  • 15
    • 0029015447 scopus 로고
    • Interest in genetic testing among first-degree relatives of breast cancer patients
    • Lerman C, Seay J, Balshem A, et al. Interest in genetic testing among first-degree relatives of breast cancer patients. Am J Med Genet. 1995;57:385-392.
    • (1995) Am J Med Genet , vol.57 , pp. 385-392
    • Lerman, C.1    Seay, J.2    Balshem, A.3
  • 16
    • 0029411046 scopus 로고
    • BRCA1 discovery aftermath: No rush for genetic testing
    • Kuska B. BRCA1 discovery aftermath: No rush for genetic testing. J Natl Cancer Inst. 1995;87:1578-1579.
    • (1995) J Natl Cancer Inst , vol.87 , pp. 1578-1579
    • Kuska, B.1
  • 17
    • 0030019446 scopus 로고    scopus 로고
    • Attitudes of 47 mothers of pediatric oncology patients toward genetic testing for cancer predisposition
    • Patenaude AF, Basili L, Fairclough DL, et al. Attitudes of 47 mothers of pediatric oncology patients toward genetic testing for cancer predisposition. J Clin Oncol. 1996;14:415-421.
    • (1996) J Clin Oncol , vol.14 , pp. 415-421
    • Patenaude, A.F.1    Basili, L.2    Fairclough, D.L.3
  • 18
    • 13344260688 scopus 로고    scopus 로고
    • Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer
    • FitzGerald MG, MacDonald DJ, Krainer M, et al. Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer. N Engl J Med. 1996;334:143-149.
    • (1996) N Engl J Med , vol.334 , pp. 143-149
    • FitzGerald, M.G.1    MacDonald, D.J.2    Krainer, M.3
  • 19
    • 0030049823 scopus 로고    scopus 로고
    • BRCA1 mutations in a population-based sample of young women with breast cancer
    • Langston AA, Malone KE, Thompson JD, et al BRCA1 mutations in a population-based sample of young women with breast cancer. N Engl J Med. 1996;334:137-142.
    • (1996) N Engl J Med , vol.334 , pp. 137-142
    • Langston, A.A.1    Malone, K.E.2    Thompson, J.D.3
  • 20
    • 10544228553 scopus 로고    scopus 로고
    • Findings on breast cancer have only complicated the puzzle: Research into genes raises many hopes and many questions
    • 04/30/96
    • Grady, D. Findings on breast cancer have only complicated the puzzle: Research into genes raises many hopes and many questions. New York Times 04/30/96, B9.
    • New York Times
    • Grady, D.1
  • 21
    • 0027517995 scopus 로고
    • Correlation between genotype and phenotype in patients with cystic fibrosis
    • Cystic Fibrosis Genotype-Phenotype Consortium. Correlation between genotype and phenotype in patients with cystic fibrosis. Written by A. Hamosh and M. Corey. N Engl J Med. 1993;329:1308-1313.
    • (1993) N Engl J Med , vol.329 , pp. 1308-1313
    • Hamosh, A.1    Corey, M.2
  • 22
    • 0028779530 scopus 로고
    • Correlation between genotype and phenotype in patients with cystic fibrosis
    • Hamosh A, Corey M. Correlation between genotype and phenotype in patients with cystic fibrosis. N Engl J Med. 1994;329:866-867.
    • (1994) N Engl J Med , vol.329 , pp. 866-867
    • Hamosh, A.1    Corey, M.2
  • 23
    • 0025967994 scopus 로고
    • Association of less common cystic fibrosis mutations with a mild phenotype
    • Curtis A, Nelson R, Porteous M, et al. Association of less common cystic fibrosis mutations with a mild phenotype. J Med Genet. 1991;28:34-37.
    • (1991) J Med Genet , vol.28 , pp. 34-37
    • Curtis, A.1    Nelson, R.2    Porteous, M.3
  • 24
    • 0028325519 scopus 로고
    • Correlation between genotype and phenotype in patients with cystic fibrosis
    • Can KH, Heijrman HGM, Bakker W. Correlation between genotype and phenotype in patients with cystic fibrosis. N Engl J Med. 1994;330:865-866.
    • (1994) N Engl J Med , vol.330 , pp. 865-866
    • Can, K.H.1    Heijrman, H.G.M.2    Bakker, W.3
  • 25
    • 0025284532 scopus 로고
    • Linked marker haplotypes and the delta F508 mutation in adults with mild pulmonary disease and cystic fibrosis
    • Santis G, Osborne L, Knight RA, et al. Linked marker haplotypes and the delta F508 mutation in adults with mild pulmonary disease and cystic fibrosis. Lancet. 1990a;335:1426-1429.
    • (1990) Lancet , vol.335 , pp. 1426-1429
    • Santis, G.1    Osborne, L.2    Knight, R.A.3
  • 26
    • 0027051374 scopus 로고
    • Severity of chest disease in cystic fibrosis patients in relation to their genotypes
    • al-Jader LN, Meredith AL, Ryley HC, et al. Severity of chest disease in cystic fibrosis patients in relation to their genotypes. J Med Genet. 1992;29:883-887.
    • (1992) J Med Genet , vol.29 , pp. 883-887
    • Al-Jader, L.N.1    Meredith, A.L.2    Ryley, H.C.3
  • 27
    • 0025011995 scopus 로고
    • Independent genetic determinants of pancreatic and pulmonary status in cystic fibrosis
    • Santis G, Osborne L, Knight RA, et al. Independent genetic determinants of pancreatic and pulmonary status in cystic fibrosis. Lancet. 1990b;336:1081-1084.
    • (1990) Lancet , vol.336 , pp. 1081-1084
    • Santis, G.1    Osborne, L.2    Knight, R.A.3
  • 28
    • 0026780377 scopus 로고
    • Genotype/phenotype association in cystic fibrosis: Analyses of the delta F508, R553X, and 3905insT mutations
    • Liechti-Gallati S, Bonsall I, Malik N, et al. Genotype/phenotype association in cystic fibrosis: analyses of the delta F508, R553X, and 3905insT mutations. Pediatr Res. 1992;32:175-178.
    • (1992) Pediatr Res , vol.32 , pp. 175-178
    • Liechti-Gallati, S.1    Bonsall, I.2    Malik, N.3
  • 29
    • 0027328359 scopus 로고
    • Legal and regulatory issues surrounding carrier testing
    • Charo RA. Legal and regulatory issues surrounding carrier testing. Clin Obstet Gynecol. 1993;36:568-597.
    • (1993) Clin Obstet Gynecol , vol.36 , pp. 568-597
    • Charo, R.A.1
  • 30
    • 0026620941 scopus 로고
    • The introduction of cystic fibrosis carrier screening into clinical practice: Policy considerations
    • Wilfond BS,Fost N. The introduction of cystic fibrosis carrier screening into clinical practice: Policy considerations. The Milbank Quarterly. 1992;70:629-659.
    • (1992) The Milbank Quarterly , vol.70 , pp. 629-659
    • Wilfond, B.S.1    Fost, N.2
  • 31
    • 0027465404 scopus 로고
    • Genetic counseling for families with inherited susceptibility to breast and ovarian cancer
    • Biesecker BB, Boehnke M, Calzone, K, et al. 1993. Genetic counseling for families with inherited susceptibility to breast and ovarian cancer. JAMA. 1993;269:1970-1974.
    • (1993) JAMA , vol.269 , pp. 1970-1974
    • Biesecker, B.B.1    Boehnke, M.2    Calzone, K.3
  • 32
    • 34249840590 scopus 로고
    • Presymptomatic testing for adult-onset genetic disease: Recommendations for counseling
    • Quaid K. Presymptomatic testing for adult-onset genetic disease: recommendations for counseling. J Genet Counsel. 1992;1:277-302.
    • (1992) J Genet Counsel , vol.1 , pp. 277-302
    • Quaid, K.1
  • 33
    • 0023478473 scopus 로고
    • Performance of breast self-examination by women at high risk for breast cancer
    • Alagna SW, Morokoff PJ, Bevett JM, et al. Performance of breast self-examination by women at high risk for breast cancer. Women & Health. 1987;12:29-46.
    • (1987) Women & Health , vol.12 , pp. 29-46
    • Alagna, S.W.1    Morokoff, P.J.2    Bevett, J.M.3
  • 34
    • 0027280593 scopus 로고
    • Mammography adherence and psychological distress among women at risk for breast cancer
    • Lerman C, Daly M, Sands C, et al. Mammography adherence and psychological distress among women at risk for breast cancer. J Natl Cancer Inst. 1993;85:1074-1080.
    • (1993) J Natl Cancer Inst , vol.85 , pp. 1074-1080
    • Lerman, C.1    Daly, M.2    Sands, C.3
  • 35
    • 0026609094 scopus 로고
    • Discrimination as a consequence of genetic testing
    • Billings PR, Kohn MA, de Cuevas M, et al. Discrimination as a consequence of genetic testing. Am J Hum Genet. 1992;50:476-482.
    • (1992) Am J Hum Genet , vol.50 , pp. 476-482
    • Billings, P.R.1    Kohn, M.A.2    De Cuevas, M.3
  • 36
    • 0026655732 scopus 로고
    • A survey of state insurance commissioners concerning genetic testing and life insurance
    • McEwen JE, McArty K, Reilly PR. A survey of state insurance commissioners concerning genetic testing and life insurance. Am J Hum Genet. 1992;51:785-792.
    • (1992) Am J Hum Genet , vol.51 , pp. 785-792
    • McEwen, J.E.1    McArty, K.2    Reilly, P.R.3
  • 38
    • 0028813762 scopus 로고
    • Genetic testing and insurance. The Ad Hoc Committee on Genetic Testing/Insurance Issues
    • Anonymous. Genetic testing and insurance. The Ad Hoc Committee on Genetic Testing/Insurance Issues. Am J Hum Genet. 1995;56:327-331.
    • (1995) Am J Hum Genet , vol.56 , pp. 327-331
  • 39
    • 0025939641 scopus 로고
    • Use of genetic testing by employers
    • Council on Ethical and Judicial Affairs of the American Medical Association. Use of genetic testing by employers. JAMA. 1991;266:1827-1830.
    • (1991) JAMA , vol.266 , pp. 1827-1830
  • 41
    • 84985200193 scopus 로고
    • Discrimination and disability: The challenges to the ADA
    • Parmet WE. Discrimination and disability: the challenges to the ADA. Law, Medicine, & Health Care. 1990;18:331-344.
    • (1990) Law, Medicine, & Health Care , vol.18 , pp. 331-344
    • Parmet, W.E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.