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- 2021
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Mark
Opportunistic genomic screening. Recommendations of the European Society of Human Genetics
(
- Contribution to journal › Article
- 2018
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Mark
The challenges of the expanded availability of genomic information : an agenda-setting paper
(
- Contribution to journal › Article
- 2015
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Mark
Whole-genome sequencing in newborn screening? : A statement on the continued importance of targeted approaches in newborn screening programmes
(
- Contribution to journal › Article
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Mark
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.
(
- Contribution to journal › Article
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Mark
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
2015) In European Journal of Human Genetics(
- Contribution to journal › Article
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Mark
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
(
- Contribution to journal › Article
- 2012
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Mark
The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe
(
- Contribution to journal › Article
- 2011
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Mark
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 disorders
(
- Contribution to journal › Article
- 2009
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Mark
Testing the Children: Do Non-Genetic Health-Care Providers Differ in Their Decision to Advise Genetic Presymptomatic Testing on Minors? A Cross-Sectional Study in Five Countries in the European Union
(
- Contribution to journal › Article