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- 2020
-
Mark
It's much more grey than black and white : clinical geneticists' views on the oversight of consumer genomics in Europe
(
- Contribution to journal › Article
-
Mark
Communicating genetic information to family members : analysis of consent forms for diagnostic genomic sequencing
(
- Contribution to journal › Article
- 2018
-
Mark
Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms
(
- Contribution to journal › Article
-
Mark
Readability of informed consent forms for whole-exome and whole-genome sequencing
(
- Contribution to journal › Article
-
Mark
The challenges of the expanded availability of genomic information : an agenda-setting paper
(
- Contribution to journal › Article
- 2017
-
Mark
Regulating the advertising of genetic tests in Europe : a balancing act
(
- Contribution to journal › Article
- 2016
-
Mark
Content Analysis of Informed Consent for Whole Genome Sequencing Offered by Direct-to-Consumer Genetic Testing Companies
(
- Contribution to journal › Article
- 2015
-
Mark
Current Ethical Issues Related to the Implementation of Whole-Exome and Whole-Genome Sequencing
2015) p.481-497(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Whole-genome sequencing in newborn screening? : A statement on the continued importance of targeted approaches in newborn screening programmes
(
- Contribution to journal › Article
-
Mark
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.
(
- Contribution to journal › Article