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1.
Guidelines on ethical issues in medical genetics and the provision of genetics services / prepared by Dorothy C. Wertz, John C. Fletcher, Kare Berg in cooperation with the World Health Organization, Victor Boulyjenkov
Wertz, Dorothy C; Fletcher, John C; Berg, Kare; Boulyjenkov, Victor; World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1995. (WHO/HDP/GL/ETH/95.1. Unpublished).
in English | WHO IRIS | ID: who-62048

Subject(s)
Genetics, Medical , Ethics, Medical , Guideline , Genetic Diseases, Inborn
2.
Non-invasive screening for prenatal genetic diagnosis : report of a WHO temporary adviser / by J. L. Simpson
Simpson, J. L; World Health Organization. Hereditary Diseases Programme; International Working Group on Non-Invasive Screening for Prenatal Genetic Diagnosis (1994 : Tel Aviv, Israel).
Geneva; World Health Organization; 1995. (WHO/HDP/CONS/95.3. Unpublished).
in English | WHO IRIS | ID: who-61334

Subject(s)
Genetic Diseases, Inborn , Genetic Testing , Prenatal Diagnosis , Ultrasonography, Prenatal
3.
Summary statement on ethical issues in medical genetics : report of WHO temporary advisers / Dorothy C. Wertz, John C. Fletcher, Kare Berg
Wertz, Dorothy C; Fletcher, John C; Berg, Kare; World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1995. (WHO/HDP/GL/ETH.SUM/95.2. Unpublished).
in English | WHO IRIS | ID: who-61111

Subject(s)
Genetics, Medical , Ethics, Medical , Guideline , Genetic Diseases, Inborn
4.
Educational materials on prenatal diagnosis for sickle cell disorder / Educational materials on prenatal diagnosis for sickle cell disorder
World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1994. 21 p. (WHO/HDP/EM/PN.SCD/94.2).
Monography in English | PAHO | ID: pah-19516

Subject(s)
Hemoglobin SC Disease/diagnosis , Teaching Materials
5.
Guidelines for the control of haemoglobin disorders / edited by Bernadette Modell
Modell, Bernadette; World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1994. (WHO/HDP/HB/GL/94.1).
in English | WHO IRIS | ID: who-66665

Subject(s)
Hemoglobinopathies , Guideline
6.
Educational materials on prenatal diagnosis for sickle cell disorder
World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1994. (WHO/HDP/EM/PN.SCD/94.2 Unpublished).
in English | WHO IRIS | ID: who-62480

Subject(s)
Hemoglobin SC Disease , Teaching Materials , Sickle Cell Trait
7.
Report of a Joint WHO/WFH Meeting on the Control of Haemophilia : modern treatment of haemophilia, Geneva, 21-23 March 1994
Joint WHO/WFH Meeting on the Control of Haemophilia: Modern Treatment of Haemophilia (1994: Geneva, Switzerland); World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1994. (WHO/HDP/WFH/94.6. Unpublished).
in English | WHO IRIS | ID: who-59061

Subject(s)
Hemophilia A
8.
Educational materials on haemoglobinopathies : alpha zero thalassaemia (restricted for clinicians and for distribution via DNA laboratories only / prepared by Bernadette Modell on behalf of WHO
Modell, Bernadette; World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1994. (WHO/HDP/EM/HB.AZT/94.3. Unpublished).
in English | WHO IRIS | ID: who-59056

Subject(s)
Hemoglobinopathies , alpha-Thalassemia , Teaching Materials
9.
Educational materials on haemoglobinopathies : beta thalassaemia / prepared by Bernadette Modell on behalf of WHO
Modell, Bernadette; World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1994. (WHO/HDP/EM/HB.BT/94.5. Unpublished).
in English | WHO IRIS | ID: who-59053

Subject(s)
Hemoglobinopathies , beta-Thalassemia , Teaching Materials
10.
Educational materials on haemoglobinopathies : alpha thalassaemia / prepared by Bernadette Modell
Modell, Bernadette; World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1994. (WHO/HDP/EM/HB.AT/94.4. Unpublished).
in English | WHO IRIS | ID: who-58850

Subject(s)
Hemoglobinopathies , alpha-Thalassemia , Teaching Materials
11.
Joint WHO/TIF Meeting on the Prevention and Control of Haemoglobinopathies : 7th Meeting of the WHO Working Group on the Control of Hereditary Anaemias
Joint WHO/TIF Meeting on the Prevention and Control of Haemoglobinopathies (1993: Nicosia, Cyprus); World Health Organization. Hereditary Diseases Programme; WHO Working Group on the Control of Hereditary Anaemias. Meeting . (7th : 1993 : Nicosia, Cyprus).
Geneva; World Health Organization; 1993. (WHO/HDP/TIF/HA/93.1. Unpublished).
| WHO IRIS | ID: who-62495

Subject(s)
Hemoglobinopathies , Guideline , Teaching Materials
12.
Report of a Joint WHO/Hemochromatosis Foundation/French Hemochromatosis Association Meeting on the Prevention and Control of Hemochromatosis
Joint WHO/Hemochromatosis Foundation/French Hemochromatosis Meeting on the Prevention and Control of Hemochromatosis (1993: Kiryat, Anavim, Israel); World Health Organization. Hereditary Diseases Programme; Hemochromatosis Foundation; French Hemochromatosis Association.
Geneva; World Health Organization; 1993. (WHO/HDP/HF/FHA/93.2. Unpublished).
in English | WHO IRIS | ID: who-62491

Subject(s)
Hemochromatosis
13.
Guidelines for the development of national programmes for monitoring birth defects / prepared by the International Centre for Birth Defects of the International Clearinghouse for Birth Defects Monitoring Systems (ICBDMS)
International Clearinghouse for Birth Defects Monitoring Systems . International Centre for Birth Defects; World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1993. (WHO/HDP/ICBDMS/GL/93.4).
in English | WHO IRIS | ID: who-61536

Subject(s)
Genetic Diseases, Inborn , Congenital Abnormalities , Data Collection , Registries , Hungary , Developing Countries
14.
Report of a WHO/National Neurofibromatosis Foundation Meeting on the Control of Neurofibromatosis : National/International Management
Joint WHO/National Neurofibromatosis Foundation Meeting on the Control of Neurofibromatosis: National/International Management (1992 : Vienna, Austria); World Health Organization. Hereditary Diseases Programme; National Neurofibromatosis Foundation (U.S.).
Geneva; World Health Organization; 1992. (WHO/HDP/NNFF/WG/92.6. Unpublished).
in English | WHO IRIS | ID: who-62493

Subject(s)
Neurofibromatoses
15.
Report of a joint WHO/WFH meeting on the control of haemophilia : carrier detection and prenatal diagnosis
World Health Organization. Hereditary Diseases Programme; World Federation of Haemophilia.
Geneva; World Health Organization; 1992. (WHO/HDP/WFH/92.4. Unpublished).
in English | WHO IRIS | ID: who-62203

Subject(s)
Hemophilia A , Heterozygote , Prenatal Diagnosis , Genetic Carrier Screening
16.
Ethical, legal and social issues of the human genome project : report of a WHO temporary adviser / by D. F. Roberts
Roberts, Derek Frank; World Health Organization. Hereditary Diseases Programme; Conference on the Ethical Legal and Social Issues of Human Genome Research (1992 : Fukui, Japan).
Geneva; World Health Organization; 1992. (WHO/HDP/CONS/92.8. Unpublished).
in English | WHO IRIS | ID: who-62196

Subject(s)
Bioethics , Genetics, Medical , Human Genome Project
17.
Joint WHO/ICF(MA Meeting on the Possibilities for the Treatment of Cystic Fibrosis, Washington, D.C., USA, 14 October 1992 : report
Joint WHO/ICF(M)A Meeting on the Possibilities for the Treatment of Cystic Fibrosis 1992: Washington, D.C., USA); World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1992. (WHO/HDP/ICF(M)A/WG/92.7. Unpublished).
in English | WHO IRIS | ID: who-62081

Subject(s)
Cystic Fibrosis
18.
Current trends in early prenatal diagnosis : report of a WHO temporary adviser / by Bernadette Modell
Modell, Bernadette; World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1992. (WHO/HDP/CONS/92.5. Unpublished).
in English | WHO IRIS | ID: who-61933

Subject(s)
Prenatal Diagnosis
19.
Current trends in hereditary diseases : research and management , report of a WHO temporary adviser / Vladimir I. Ivanov
Ivanov, Vladimir I; World Health Organization. Hereditary Diseases Programme.
Geneva; World Health Organization; 1992. (WHO/HDP/CONS/92.3. Unpublished).
in English | WHO IRIS | ID: who-61341

Subject(s)
Genetics, Medical , Genetic Diseases, Inborn
20.
Educational information about haemophilia for families / prepared by members of the Medical Advisory Board, World Federation of Hemophilia, in particular, E. Berry, M. Hilgartner, and reviewed by P. Jones
Berry, E; Hilgartner, M; Jones, P; World Health Organization. Hereditary Diseases Programme; World Federation of Hemophilia; Joint WHO/WFH Meeting on the Possibilities for the Prevention and Control of Haemophilia (1990 : Geneva, Switzerland).
Geneva; World Health Organization; 1992. (WHO/HDP/HAEM/EMT/92.1. Unpublished).
in English | WHO IRIS | ID: who-60836

Subject(s)
Hemophilia A
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