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Volumn , Issue 865, 1996, Pages

Control of hereditary diseases
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EID: 17444449933     PISSN: 05123054     EISSN: None     Source Type: Book Series    
DOI: None     Document Type: Article
Times cited : (7)

References (52)
  • 2
    • 2342652856 scopus 로고
    • Demography, vital statistics and the pattern of disease in childhood
    • Campbell AGM, McIntosh N, eds. Edinburgh, Churchill Livingstone
    • Forfar JO. Demography, vital statistics and the pattern of disease in childhood. In: Campbell AGM, McIntosh N, eds. Forfar and Arniel's textbook of paediatrics, 4th ed. Edinburgh, Churchill Livingstone, 1992.
    • (1992) Forfar and Arniel's Textbook of Paediatrics, 4th Ed.
    • Forfar, J.O.1
  • 3
    • 0004018975 scopus 로고
    • Report of a WHO Advisory Group on Hereditary Diseases. Geneva, World Health Organization, unpublished document HMG/WG/85.10, available on request from Human Genetics, World Health Organization, 1211 Geneva 27, Switzerland
    • Community approaches to the control of hereditary diseases. Report of a WHO Advisory Group on Hereditary Diseases. Geneva, World Health Organization, 1985 (unpublished document HMG/WG/85.10, available on request from Human Genetics, World Health Organization, 1211 Geneva 27, Switzerland).
    • (1985) Community Approaches to the Control of Hereditary Diseases
  • 4
    • 0023936538 scopus 로고
    • Genetic disorders in children and young adults: A population study
    • Baird PA et al. Genetic disorders in children and young adults: a population study. American journal of human genetics, 1988, 42:677-693.
    • (1988) American Journal of Human Genetics , vol.42 , pp. 677-693
    • Baird, P.A.1
  • 5
    • 0021134039 scopus 로고
    • The load of genetic and partly genetic disorders in man. 1. Congenital anomalies: Estimates of detriment in terms of years of life lost and years of impaired life
    • Czeizel A, Sankaranarayanan K. The load of genetic and partly genetic disorders in man. 1. Congenital anomalies: estimates of detriment in terms of years of life lost and years of impaired life. Mutation research, 1984, 128: 73-103.
    • (1984) Mutation Research , vol.128 , pp. 73-103
    • Czeizel, A.1    Sankaranarayanan, K.2
  • 6
    • 0004093959 scopus 로고
    • Copenhagen, World Health Organization, Regional Office for Europe, WHO Regional Publication, European Series No. 38
    • Modell B, Kuliev AM, Wagner M. Community genetics services in Europe. Copenhagen, World Health Organization, Regional Office for Europe, 1992 (WHO Regional Publication, European Series No. 38).
    • (1992) Community Genetics Services in Europe
    • Modell, B.1    Kuliev, A.M.2    Wagner, M.3
  • 8
    • 0024951961 scopus 로고
    • Glucose-6-phosphate dehydrogenase deficiency. Report of a WHO Working Group
    • Glucose-6-phosphate dehydrogenase deficiency. Report of a WHO Working Group. Bulletin of the World Health Organization 1989, 67:601-611.
    • (1989) Bulletin of the World Health Organization , vol.67 , pp. 601-611
  • 9
    • 0003393882 scopus 로고
    • Geneva, World Health Organization, unpublished document WHO/HDP/HB/GL794.1, available on request from Human Genetics, World Health Organization, 1211 Geneva 27, Switzerland
    • Guidelines for the control of haemoglobin disorders. Geneva, World Health Organization, 1994 (unpublished document WHO/HDP/HB/GL794.1, available on request from Human Genetics, World Health Organization, 1211 Geneva 27, Switzerland).
    • (1994) Guidelines for the Control of Haemoglobin Disorders
  • 12
    • 2342449234 scopus 로고
    • Geneva, World Health Organization, unpublished document WHO/HDP/ADV/89.3, available on request from Human Genetics, World Health Organization, 1211 Geneva 27, Switzerland
    • Advances in diagnosis, treatment and prevention of hereditary diseases. Report of a World Health Organization meeting. Geneva, World Health Organization, 1989 (unpublished document WHO/HDP/ADV/89.3, available on request from Human Genetics, World Health Organization, 1211 Geneva 27, Switzerland).
    • (1989) Advances in Diagnosis, Treatment and Prevention of Hereditary Diseases. Report of a World Health Organization Meeting
  • 13
    • 0027416952 scopus 로고
    • What proportion of congenital anomalies can be prevented?
    • Czeizel A, Intody Z, Modell B. What proportion of congenital anomalies can be prevented? British medical journal, 1993, 306:499-502.
    • (1993) British Medical Journal , vol.306 , pp. 499-502
    • Czeizel, A.1    Intody, Z.2    Modell, B.3
  • 14
    • 0024508882 scopus 로고
    • Incidence of congenital rubella syndrome in 19 regions of Europe in 1980-1986
    • de la Mata I et al. Incidence of congenital rubella syndrome in 19 regions of Europe in 1980-1986. European journal of epidemiology, 1989, 5:106-109.
    • (1989) European Journal of Epidemiology , vol.5 , pp. 106-109
    • De La Mata, I.1
  • 15
    • 0025863475 scopus 로고
    • Prevention of neural tube defects: Results of the Medical Research Council vitamin study
    • MRC Vitamin Research Group. Prevention of neural tube defects: results of the Medical Research Council vitamin study. Lancet, 1991, 338:131-137.
    • (1991) Lancet , vol.338 , pp. 131-137
  • 16
    • 0025063290 scopus 로고
    • Carrier testing and prenatal diagnosis for hemophilia: Experiences and attitudes of 549 potential and obligate carriers
    • Varekamp I et al. Carrier testing and prenatal diagnosis for hemophilia: experiences and attitudes of 549 potential and obligate carriers. American journal of medical genetics, 1990, 37:147-154.
    • (1990) American Journal of Medical Genetics , vol.37 , pp. 147-154
    • Varekamp, I.1
  • 17
    • 0002431469 scopus 로고
    • Principles of screening
    • NJ Wald, ed. Oxford, Oxford University Press
    • Cuckle HS, Wald NJ. Principles of screening. In: NJ Wald, ed. Antenatal and neonatal screening. Oxford, Oxford University Press, 1984.
    • (1984) Antenatal and Neonatal Screening
    • Cuckle, H.S.1    Wald, N.J.2
  • 18
    • 0027360434 scopus 로고
    • Tay-Sachs disease - Carrier screening, prenatal diagnosis, and the molecular era. An international perspective 1970-1993
    • Kaback M et al. Tay-Sachs disease - carrier screening, prenatal diagnosis, and the molecular era. An international perspective 1970-1993. Journal of the American Medical Association, 1993, 270:2307-2315.
    • (1993) Journal of the American Medical Association , vol.270 , pp. 2307-2315
    • Kaback, M.1
  • 19
    • 0025166739 scopus 로고
    • Comparison of audible sound transmission with ultrasound in screening for congenital dislocation of the hip
    • Stone MH et al. Comparison of audible sound transmission with ultrasound in screening for congenital dislocation of the hip. Lancet, 1990, 336:421-422.
    • (1990) Lancet , vol.336 , pp. 421-422
    • Stone, M.H.1
  • 20
    • 0023242288 scopus 로고
    • Mental development in congenital hypothyroidism after neonatal screening
    • Illig R et al. Mental development in congenital hypothyroidism after neonatal screening. Archives of disease in childhood, 1987, 62:1050-1055.
    • (1987) Archives of Disease in Childhood , vol.62 , pp. 1050-1055
    • Illig, R.1
  • 21
    • 0024654902 scopus 로고
    • Neonatal screening for sickle cell disease
    • Neonatal screening for sickle cell disease. Paediatrics, 1989, 83 (Suppl.).
    • (1989) Paediatrics , vol.83 , Issue.SUPPL.
  • 22
    • 0029130343 scopus 로고
    • The impact of newborn screening on cystic fibrosis testing in Victoria, Australia
    • Balnaves ME et al. The impact of newborn screening on cystic fibrosis testing in Victoria, Australia. Journal of medical genetics, 1995, 32:537-542.
    • (1995) Journal of Medical Genetics , vol.32 , pp. 537-542
    • Balnaves, M.E.1
  • 23
    • 0024355277 scopus 로고
    • Screening for Duchenne muscular dystrophy
    • Smith RA et al. Screening for Duchenne muscular dystrophy. Archives of disease in childhood, 1989, 64:1017-1021.
    • (1989) Archives of Disease in Childhood , vol.64 , pp. 1017-1021
    • Smith, R.A.1
  • 24
    • 0026692180 scopus 로고
    • Antenatal maternal serum screening for Down's syndrome: Results of a demonstration study
    • Wald NJ et al. Antenatal maternal serum screening for Down's syndrome: results of a demonstration study. British medical journal, 1992, 305:391-393.
    • (1992) British Medical Journal , vol.305 , pp. 391-393
    • Wald, N.J.1
  • 26
    • 0027298758 scopus 로고
    • Prevention of congenital abnormalities by periconceptional multivitamin supplementation
    • Czeizel AE. Prevention of congenital abnormalities by periconceptional multivitamin supplementation. British medical journal, 1993, 306:1645-8.
    • (1993) British Medical Journal , vol.306 , pp. 1645-1648
    • Czeizel, A.E.1
  • 27
    • 0024426983 scopus 로고
    • Uptake of presymptomatic predictive testing for Huntington's disease
    • Craufurd D et al. Uptake of presymptomatic predictive testing for Huntington's disease. Lancet, 1989, ii:603-605.
    • (1989) Lancet , vol.2 , pp. 603-605
    • Craufurd, D.1
  • 28
    • 0025194995 scopus 로고
    • Thalassaemia in Bombay: The role of medical genetics in developing countries
    • Sangani B et al. Thalassaemia in Bombay: the role of medical genetics in developing countries. Bulletin of the World Health Organization, 1990, 68:75-81.
    • (1990) Bulletin of the World Health Organization , vol.68 , pp. 75-81
    • Sangani, B.1
  • 29
    • 0021919667 scopus 로고
    • Ethical aspects of medical genetics. A proposal for guidelines in genetic counselling, prenatal diagnosis and screening
    • Fletcher JC, Berg K, Tranoy KE. Ethical aspects of medical genetics. A proposal for guidelines in genetic counselling, prenatal diagnosis and screening. Clinical genetics, 1985, 27:199-205.
    • (1985) Clinical Genetics , vol.27 , pp. 199-205
    • Fletcher, J.C.1    Berg, K.2    Tranoy, K.E.3
  • 31
    • 2342541679 scopus 로고
    • Acceptance of first trimester prenatal diagnosis: Analysis of the religious and socio-cultural characteristics
    • Tului L, Brambati B. Acceptance of first trimester prenatal diagnosis: analysis of the religious and socio-cultural characteristics. Rivista di ostetrica, ginecologia pratica e medicina perinatale, 1990, 5:129-137.
    • (1990) Rivista di Ostetrica, Ginecologia Pratica e Medicina Perinatale , vol.5 , pp. 129-137
    • Tului, L.1    Brambati, B.2
  • 33
    • 0026529571 scopus 로고
    • Value of routine ultrasound scanning at 19 weeks: A four-year study of 8849 deliveries
    • Luck CA. Value of routine ultrasound scanning at 19 weeks: a four-year study of 8849 deliveries. British medical journal, 1992, 304:1474-1476.
    • (1992) British Medical Journal , vol.304 , pp. 1474-1476
    • Luck, C.A.1
  • 35
    • 84982671631 scopus 로고
    • Randomized study of early amniocentesis versus chorionic villus sampling: A technical and cytogenetic comparison of 650 patients
    • Byrne D et al. Randomized study of early amniocentesis versus chorionic villus sampling: a technical and cytogenetic comparison of 650 patients. Ultrasound obstetrics and gynecology, 1991, 1:235-240.
    • (1991) Ultrasound Obstetrics and Gynecology , vol.1 , pp. 235-240
    • Byrne, D.1
  • 36
    • 0024491242 scopus 로고
    • Multicentre randomised clinical trial of chorion villus sampling and amniocentesis. First report
    • Canadian Collaborative CVS-Amniocentesis Clinical Trial Group. Multicentre randomised clinical trial of chorion villus sampling and amniocentesis. First report. Lancet, 1989, i:1-6.
    • (1989) Lancet , vol.1 , pp. 1-6
  • 37
    • 0025767956 scopus 로고
    • Medical Research Council European trial of chorion villus sampling
    • Medical Research Council Working Party on the Evaluation of Chorion Villus Sampling. Medical Research Council European trial of chorion villus sampling. Lancet, 1991, 337:1491-1499.
    • (1991) Lancet , vol.337 , pp. 1491-1499
  • 38
    • 0026101241 scopus 로고
    • Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation
    • Firth HV et al. Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation. Lancet, 1991, 337:762-763.
    • (1991) Lancet , vol.337 , pp. 762-763
    • Firth, H.V.1
  • 40
    • 0027232847 scopus 로고
    • Erythroid-specific antibodies enhance detection of fetal nucleated erythrocytes in maternal blood
    • Bianchi DW et al. Erythroid-specific antibodies enhance detection of fetal nucleated erythrocytes in maternal blood. Prenatal diagnosis, 1993, 13:293-300.
    • (1993) Prenatal Diagnosis , vol.13 , pp. 293-300
    • Bianchi, D.W.1
  • 41
    • 2342655676 scopus 로고
    • Management of isoimmunization in pregnancy
    • American College of Obstetricians and Gynecologists. Management of isoimmunization in pregnancy. Technical bulletin, 1990, 148:1-6.
    • (1990) Technical Bulletin , vol.148 , pp. 1-6
  • 42
    • 0026019857 scopus 로고
    • In utero transplantation of hemopoietic stem cells in humans
    • Touraine JL et al. In utero transplantation of hemopoietic stem cells in humans. Transplantation proceedings, 1991, 23:1706-1708.
    • (1991) Transplantation Proceedings , vol.23 , pp. 1706-1708
    • Touraine, J.L.1
  • 43
    • 0027128267 scopus 로고
    • The dream of the human genome
    • Lewontin RC. The dream of the human genome. New York Times review, 1992, 28:31-40.
    • (1992) New York Times Review , vol.28 , pp. 31-40
    • Lewontin, R.C.1
  • 44
    • 0024100716 scopus 로고
    • New tools, new dilemmas: Genetic frontiers
    • Nolan K, Swenson S. New tools, new dilemmas: genetic frontiers. Hastings Center report, 1988, 18:40-46.
    • (1988) Hastings Center Report , vol.18 , pp. 40-46
    • Nolan, K.1    Swenson, S.2
  • 46
    • 0028062784 scopus 로고
    • The Human Genome Project: Under an international legal and ethical microscope
    • Knoppers BM, Chadwick R. The Human Genome Project: under an international legal and ethical microscope. Science, 1994, 265:2033-2034.
    • (1994) Science , vol.265 , pp. 2033-2034
    • Knoppers, B.M.1    Chadwick, R.2
  • 47
    • 0011684559 scopus 로고
    • The Hague, Health Council of the Netherlands
    • Committee of the Health Council of the Netherlands. Heredity: science and society. The Hague, Health Council of the Netherlands, 1989.
    • (1989) Heredity: Science and Society
  • 48
    • 0026908416 scopus 로고
    • Right not to know or duty to know? Prenatal screening for polycystic renal disease
    • Kielstein R, Sass H-M. Right not to know or duty to know? Prenatal screening for polycystic renal disease. Journal of medical philosophy, 1992, 17:395-405.
    • (1992) Journal of Medical Philosophy , vol.17 , pp. 395-405
    • Kielstein, R.1    Sass, H.-M.2
  • 49
    • 0026840247 scopus 로고
    • The double helix
    • Andrews LB. The double helix. Houston law review, 1992, 29(1):149-184.
    • (1992) Houston Law Review , vol.29 , Issue.1 , pp. 149-184
    • Andrews, L.B.1
  • 50
    • 2342591301 scopus 로고
    • R. v. Dyment, 2 SCR 417-442, 1988; Privacy Commissioner of Canada, Genetic Testing and Privacy, Minister of Supply and Services, 1992.
    • (1988) 2 SCR , pp. 417-442
    • Dyment, R.V.1
  • 51
    • 0008590696 scopus 로고
    • Minister of Supply and Services
    • R. v. Dyment, 2 SCR 417-442, 1988; Privacy Commissioner of Canada, Genetic Testing and Privacy, Minister of Supply and Services, 1992.
    • (1992) Genetic Testing and Privacy
  • 52
    • 0025444345 scopus 로고
    • Patenting the human genome
    • Eisenberg RS. Patenting the human genome. Emory law journal, 1990, 39: 721-745.
    • (1990) Emory Law Journal , vol.39 , pp. 721-745
    • Eisenberg, R.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.