28 results on '"Cornel, Martina C"'
Search Results
2. Perceptions of reproductive healthcare providers regarding their involvement in offering expanded carrier screening in fertility clinics: a qualitative study
3. Improving care for rare genetic neurodevelopmental disorders: A systematic review and critical appraisal of clinical practice guidelines using AGREE II
4. Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?
5. The impact of the Journal of Community Genetics: Good Health and Wellbeing, Quality Education, and Reduced Inequalities
6. Effectiveness of L-serine supplementation in children with a GRIN2B loss-of-function mutation: Rationale and protocol for single patient (n-of-1) multiple cross-over trials
7. New year, new goals for the journal?
8. Chapter 2 Risk Calculations in Consanguinity
9. Engagement of patients and the public in personalised prevention in Europe using genomic information: a scoping review.
10. Do we care? Reporting of genetic diagnoses in multidisciplinary intellectual disability care: a retrospective chart review.
11. Corrigendum to Effectiveness of L-serine supplementation in children with a GRIN2B loss-of-function mutation: Rationale and protocol for single patient (n-of-1) multiple cross-over trials. Contemp Clin Trials Commun. 36 (2023) Pages not provided/ DOI: 10.1016/j.conctc.2023.101233
12. Reproductive healthcare providers’ perceptions regarding their involvement in offering expanded carrier screening in fertility clinics: a qualitative study
13. Moving somatic gene editing to the clinic: routes to market access and reimbursement in Europe
14. Genetic Screening—Emerging Issues.
15. Costs, burdens and the prevention of genetic disorders: what role for professional influence?
16. Should Secondary Pharmacogenomic Variants Be Actively Screened and Reported When Diagnostic Genome-Wide Sequencing Is Performed in a Child?
17. Information Provision Regarding Health-Related Direct-to-Consumer Genetic Testing for Dutch Consumers: An in-Depth Content Analysis of Sellers' Websites.
18. Corrigendum to “Effectiveness of L-serine supplementation in children with a GRIN2B loss-of-function mutation: Rationale and protocol for single patient (n-of-1) multiple cross-over trials” [Contemp. Clin. Trials Commun. 36 (2023)/ DOI: 10.1016/j.conctc.2023.101233]
19. Chapter 26 - Community and population cardiology
20. Predictive Value of SLCO1B1 c.521T>C Polymorphism on Observed Changes in the Treatment of 1136 Statin-Users
21. Predictive Value of SLCO1B1 c.521T>C Polymorphism on Observed Changes in the Treatment of 1136 Statin-Users
22. Predictive Value of SLCO1B1 c.521T>C Polymorphism on Observed Changes in the Treatment of 1136 Statin-Users.
23. Predictive Value of c.521T>C Polymorphism on Observed Changes in the Treatment of 1136 Statin-Users
24. Dynamics of reproductive genetic technologies: Perspectives of professional stakeholders
25. Pursuing Public Health Benefit Within National Genomic Initiatives: Learning From Different Policies
26. Contributors
27. Expanding Neonatal Bloodspot Screening: A Multi-Stakeholder Perspective
28. Effectiveness of L-serine supplementation in children with a GRIN2Bloss-of-function mutation: A rationale and protocol for single patient (n-of-1) multiple cross-over trials
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