14 results on '"Fehlberg, Zoe"'
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2. Determining priority indicators of utility for genomic testing in rare disease: A Delphi study
3. Using a theory informed approach to design, execute, and evaluate implementation strategies to support offering reproductive genetic carrier screening in Australia
4. Determining the utility of diagnostic genomics: a conceptual framework
5. Scaling-up and future sustainability of a national reproductive genetic carrier screening program
6. The more you do it, the easier it gets: using behaviour change theory to support health care professionals offering reproductive genetic carrier screening
7. Early Childhood Education Participation: A Mixed-Methods Study of Parent and Provider Perceived Barriers and Facilitators
8. Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services
9. Supporting healthcare professionals to offer reproductive genetic carrier screening: a behaviour change theory approach
10. The more you do it, the easier it gets: using behaviour change theory to support health care professionals offering reproductive genetic carrier screening
11. Needs of people with rare diseases that can be supported by electronic resources: a scoping review
12. Mobile Apps for People With Rare Diseases: Review and Quality Assessment Using Mobile App Rating Scale
13. Correspondence on “Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)” by Gregg et al
14. Correspondence on “Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)” by Gregg et al
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