Informed choice in genetic screening for thalassaemia during pregnancy: audit from a national confidential inquiry. - Wikidata - awgldk - TriplyDB

Informed choice in genetic screening for thalassaemia during pregnancy: audit from a national confidential inquiry.

Informed choice in genetic screening for thalassaemia during pregnancy: audit from a national confidential inquiry.

http://www.wikidata.org/entity/Q37307614

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Iranian national thalassaemia screening programme Long-term effect of prospective detection of high genetic risk on couples' reproductive life: data for thalassaemia.Haemoglobinopathy screening can be carried out in general practice.Confidential inquiries should be funded in clinical genetics.Screening for beta thalassaemia Effectiveness of earlier antenatal screening for sickle cell disease and thalassaemia in primary care: cluster randomised trial.Antenatal screening for haemoglobinopathies in primary care: a whole system participatory action research project.Genetic Services in the Sultanate of Oman and other Gulf Countries: Progress is needed now!Acceptability of prenatal testing and termination of pregnancy in Pakistan.Risk and reproductive decisions: British Pakistani couples' responses to genetic counselling.Impact on informed choice of offering antenatal sickle cell and thalassaemia screening in primary care: a randomized trial.Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1.Falling prevalence of beta-thalassaemia and eradication of malaria in the Maldives.Carrier testing for autosomal-recessive disorders.Ethnicity and the politics of the new genetics: principles and engagement.Population genetic screening programmes: principles, techniques, practices, and policies.Timeline: Raising the profile of genetics in primary care.Delay between pregnancy confirmation and sickle cell and [corrected] thalassaemia screening: a population-based cohort study.Parents' experiences of universal screening for haemoglobin disorders: implications for practice in a new genetics era.Examining the family-centred approach to genetic testing and counselling among UK Pakistanis: a community perspective.Global epidemiology of haemoglobin disorders and derived service indicators.Prenatal Diagnosis of Different Polymorphisms of β-globin Gene in Ahvaz.A systematic review of issues around antenatal screening and prenatal diagnostic testing for genetic disorders: women of Asian origin in western countries.An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project.Attitudes towards genetic diagnosis in Pakistan: a survey of medical and legal communities and parents of thalassemic children.Public experiences, knowledge and expectations about medical genetics and the use of genetic information.Effectiveness of Prenatal Screening for Hemoglobinopathies in a Developing Country.Inclusion of diverse populations in genomic research and health services: Genomix workshop report.Haemoglobinopathy screening: an end to institutional racism?Lessons from thalassaemia screening in Iran.A national screening policy for sickle cell disease and thalassaemia major for the United Kingdom. Questions are left after two evidence based reports Meckel-Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research Advances.Three-month follow-up of Western and non-Western participants in a study on preconceptional ancestry-based carrier couple screening for cystic fibrosis and hemoglobinopathies in the Netherlands.Guidelines-based indicators to measure quality of antenatal care.The impact of migrations on the health services for rare diseases in Europe: the example of haemoglobin disorders.

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Informed choice in genetic screening for thalassaemia during pregnancy: audit from a national confidential inquiry.

http://www.wikidata.org/entity/Q37307614

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article scientifique

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bilimsel makale

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scientific article published on February 2000

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vetenskaplig artikel

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Informed choice in genetic scr ...... national confidential inquiry.

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Informed choice in genetic scr ...... national confidential inquiry.

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Informed choice in genetic scr ...... national confidential inquiry.

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Informed choice in genetic scr ...... national confidential inquiry.

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Informed choice in genetic scr ...... national confidential inquiry.

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P2860

National Confidential Enquiry into counselling for genetic disorders by non-geneticists: general recommendations and specific standards for improving care.

A multidisciplinary approach for improving services in primary care: randomised controlled trial of screening for haemoglobin disorders.

Audit of process of antenatal screening for sickle cell disorders at a north London hospital.

Audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: the first 20 years.

Prenatal screening for haemoglobin disorders.

Mapping the prevalence of sickle cell and beta thalassaemia in England: estimating and validating ethnic-specific rates.

Breaking down language barriers. The NHS needs to provide accessible interpreting services for all.

How well do we manage families with genetic problems?

Effect of fetal diagnostic testing on birth-rate of thalassaemia major in Britain.

Guideline: the laboratory diagnosis of malaria. General Haematology Task Force of the British Committee for Standards in Haematology.

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