28 results on '"Hickerton, Chriselle"'
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2. Australians’ perspectives on support around use of personal genomic testing: Findings from the Genioz study
3. Australians’ views and experience of personal genomic testing: survey findings from the Genioz study
4. Australians’ views on personal genomic testing: focus group findings from the Genioz study
5. Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes
6. “It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare
7. The expectations and realities of nutrigenomic testing in australia: A qualitative study
8. The expectations and realities of nutrigenomic testing in australia: A qualitative study
9. From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing
10. “Itʼs about having the choice”: Stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome
11. “Did you find that out in time?”: New life trajectories of parents who choose to continue a pregnancy where a genetic disorder is diagnosed or likely
12. From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing
13. 12 ‘Recreational’ consumer genomics: no such thing as a non-medical test
14. Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing
15. Personal genomic testing for nutrition and wellness in Australia: A content analysis of online information
16. Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X
17. Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screening
18. Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screening
19. Experiences of prenatal diagnosis and decision-making about termination of pregnancy: a qualitative study
20. Experiences of prenatal diagnosis and decision‐making about termination of pregnancy: A qualitative study
21. Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing.
22. A mixed methods exploration of families’ experiences of the diagnosis of childhood spinal muscular atrophy
23. ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible
24. “Did you find that out in time?”: New life trajectories of parents who choose to continue a pregnancy where a genetic disorder is diagnosed or likely
25. A mixed methods exploration of families' experiences of the diagnosis of childhood spinal muscular atrophy.
26. The expectations and realities of nutrigenomic testing in australia: A qualitative study
27. From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing.
28. Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing.
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