Population genetic screening programmes: principles, techniques, practices, and policies.
about
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disordersStakeholder attitudes towards the role and application of informed consent for newborn bloodspot screening: a study protocolAttitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening.Qualifying choice: ethical reflection on the scope of prenatal screening.Carrier screening for beta-thalassaemia: a review of international practice.Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendationsMeasuring informed choice in population-based reproductive genetic screening: a systematic review.Preconceptional genetic carrier testing and the commercial offer directly-to-consumersTay-Sachs disease: current perspectives from AustraliaAssessing the risks and benefits of diagnosing genetic conditions with variable phenotypes through population screening: Klinefelter syndrome as an example.Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making.Human genetic research: emerging trends in ethics.Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansions.Colonoscopy use following mutation detection in Lynch syndrome: exploring a role for cancer screening in adaptationCarrier screening in preconception consultation in primary care.Responsible implementation of expanded carrier screening.Attitudes of cystic fibrosis patients and parents toward carrier screening and related reproductive issues.Offering fragile X syndrome carrier screening: a prospective mixed-methods observational study comparing carrier screening of pregnant and non-pregnant women in the general populationPopulation-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases.Development of a fragile X syndrome (FXS) knowledge scale: towards a modified multidimensional measure of informed choice for FXS population carrier screening.Ethical, legal, and social issues in health technology assessment for prenatal/preconceptional and newborn screening: a workshop report.Genetic screening: a conceptual framework for programmes and policy-making.A systematic review of population screening for fragile X syndrome.Postnatal screening for Klinefelter syndrome: is there a rationale?Preventing thalassemia in Lebanon: successes and challenges in a developing country.Foetal surgery and using in utero therapies to reduce the degree of disability after birth. Could it be morally defensible or even morally required?Molecular epidemiology of citrullinemia type I in a risk region of Argentina: a first step to preconception heterozygote detection.Hemoglobinopathy carrier prevalence in the United Arab Emirates: first analysis of the Dubai Health Authority premarital screening program results.Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screening.BRCA genetic testing of individuals from families with low prevalence of cancer: experiences of carriers and implications for population screening."I'm Healthy, It's Not Going To Be Me": Exploring experiences of carriers identified through a population reproductive genetic carrier screening panel in Australia.Evaluation after five years of the cancer genetic counselling programme of Valencian Community (Eastern Spain).Conflicts regarding genetic counseling for fragile X syndrome screening: A survey of clinical geneticists and genetic counselors in IsraelBenefits and burdens of newborn screening: public understanding and decision-makingHow can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom
P2860
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P2860
Population genetic screening programmes: principles, techniques, practices, and policies.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
Population genetic screening programmes: principles, techniques, practices, and policies.
@ast
Population genetic screening programmes: principles, techniques, practices, and policies.
@en
type
label
Population genetic screening programmes: principles, techniques, practices, and policies.
@ast
Population genetic screening programmes: principles, techniques, practices, and policies.
@en
prefLabel
Population genetic screening programmes: principles, techniques, practices, and policies.
@ast
Population genetic screening programmes: principles, techniques, practices, and policies.
@en
P2093
P2860
P356
P1476
Population genetic screening programmes: principles, techniques, practices, and policies.
@en
P2093
Béatrice Godard
Gerry Evers-Kiebooms
Leo ten Kate
P2860
P2888
P304
P356
10.1038/SJ.EJHG.5201113
P478
11 Suppl 2
P577
2003-12-01T00:00:00Z