168 results on '"McClaren, Belinda"'
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2. What matters to parents? A scoping review of parents’ service experiences and needs regarding genetic testing for rare diseases
3. Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation
4. Unearthing the Learning of Genomic Medicine in the Workplace: A Qualitative Study
5. Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service delivery
6. Development and use of the Australian reproductive genetic carrier screening decision aid
7. Parents’ experiences of decision making for rapid genomic sequencing in intensive care
8. General practitioners' views on genomics, practice and education: A qualitative interview study
9. “It’s something I’ve committed to longer term”: The impact of an immersion program for physicians on adoption of genomic medicine
10. Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics
11. Which types of conditions should be included in reproductive genetic carrier screening? Views of parents of children with a genetic condition
12. Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level
13. Parental experiences after prenatal diagnosis of fetal abnormality
14. Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care
15. Embodied experiences of prenatal diagnosis of fetal abnormality and pregnancy termination
16. Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening
17. 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
18. Current practice and attitudes of Australian obstetricians toward population-based carrier screening for inherited conditions
19. 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
20. Development and use of the Australian reproductive genetic carrier screening decision aid
21. Clinical audit of genetic testing and referral patterns for fragile X and associated conditions
22. ‘A short time but a lovely little short time’: Bereaved parentsʼ experiences of having a child with spinal muscular atrophy type 1
23. The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation.
24. Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics)
25. Measuring physician practice, preparedness and preferences for genomic medicine: a national survey
26. The expectations and realities of nutrigenomic testing in australia: A qualitative study
27. Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making
28. Clinical Genomics: Integrated teamworking across the sociotechnical divide
29. The expectations and realities of nutrigenomic testing in australia: A qualitative study
30. How do individuals decide whether to accept or decline an offer of genetic testing for colorectal cancer?
31. Rapid acute care genomics: Challenges and opportunities for genetic counselors
32. HOW DO INDIVIDUALS DECIDE WHETHER TO ACCEPT OR DECLINE AN OFFER OF GENETIC TESTING FOR COLORECTAL CANCER?: Symposium 14F 3023
33. Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education
34. Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning
35. Preparing Medical Specialists to Practice Genomic Medicine: Education an Essential Part of a Broader Strategy
36. How do women at increased, but unexplained, familial risk of breast cancer perceive and manage their risk? A qualitative interview study
37. Rapid acute care genomics: Challenges and opportunities for genetic counselors.
38. Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.
39. Experiences of prenatal diagnosis and decision-making about termination of pregnancy: a qualitative study
40. Experiences of prenatal diagnosis and decision‐making about termination of pregnancy: A qualitative study
41. Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening.
42. ‘A short time but a lovely little short time’: Bereaved parents' experiences of having a child with spinal muscular atrophy type 1
43. A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy
44. A mixed methods exploration of families’ experiences of the diagnosis of childhood spinal muscular atrophy
45. Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention
46. Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research
47. In This Issue
48. Attitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening
49. Cascade carrier testing after a child is diagnosed with cystic fibrosis through newborn screening: investigating why most relatives do not have testing
50. Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making
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