762 results on '"Skirton, Heather"'
Search Results
2. The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages
3. Telling the children
4. The first competency based framework in genetics/genomics specifically for midwifery education and practice
5. Women's experiences of living with postnatal PTSD
6. An integrative review of factors that influence reproductive decisions in women with sickle cell disease
7. Presymptomatic genetic testing for hereditary cancer in young adults: a survey of young adults and parents
8. A longitudinal study of genetic counselling for families - needs, expectations and outcomes
9. Decision making and experiences of young adults undergoing presymptomatic genetic testing for familial cancer: a longitudinal grounded theory study
10. Impact of fetal or child loss on parents’ perceptions of non-invasive prenatal diagnosis for autosomal recessive conditions
11. Factors influencing the sustainability of volunteer peer support for breast-feeding mothers within a hospital environment: An exploratory qualitative study
12. Nurses' knowledge and educational needs regarding genetics
13. The evidence base regarding the experiences of and attitudes to preimplantation genetic diagnosis in prospective parents
14. A Qualitative Study to Explore the Views and Attitudes towards Prenatal Testing in Adults Who Have Muenke Syndrome and their Partners
15. The challenges of the expanded availability of genomic information: an agenda-setting paper
16. Implementing genetic education in primary care: the Gen-Equip programme
17. Ensuring Education and Quality in the Practice of Health Professionals (Non-medical) Working in Genetic Services
18. Patient Preferences for Online Person-Person Support
19. Counsellee’s experience of cancer genetic counselling with pedigrees that automatically incorporate genealogical and cancer database information
20. Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy
21. A systematic review of factors influencing uptake of invasive fetal genetic testing by pregnant women of advanced maternal age
22. Storytellers as partners in developing a genetics education resource for health professionals
23. A review assessing the current treatment strategies for postnatal psychological morbidity with a focus on post-traumatic stress disorder
24. Integrative review of cervical cancer screening in Western Asian and Middle Eastern Arab countries
25. Genetics and nursing: A whole new ball game or back to basics?
26. Direct to consumer testing in reproductive contexts – should health professionals be concerned?
27. Preparedness of newly qualified midwives to deliver clinical care: An evaluation of pre-registration midwifery education through an analysis of key events
28. Correction: The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages
29. More than an information service: are counselling skills needed by genetics professionals in the genomic era?
30. Experiences regarding maternal age-specific risks and prenatal testing of women of advanced maternal age in Japan
31. Genetic Counseling: Historical, Ethical, and Practical Aspects
32. Antenatal screening and informed choice: a cross-sectional survey of parents and professionals
33. Psychological factors that impact on women's experiences of first-time motherhood: a qualitative study of the transition
34. Genetic Counsellors : A Registration System to Assure Competence in Practice in the United Kingdom
35. Non-invasive prenatal testing for aneuploidy: a systematic review of Internet advertising to potential users by commercial companies and private health providers
36. Predictive or not predictive: understanding the mixed messages from the patientʼs DNA sequence
37. Research involving people with a learning disability - methodological challenges and ethical considerations
38. Quality of patient information leaflets for Down syndrome screening: A comparison between the UK and Thailand
39. Experiences of UK patients with hepatitis C virus infection accessing phlebotomy: A qualitative analysis
40. Building the Genetic Counsellor Profession in the United Kingdom: Two Decades of Growth and Development
41. What Counts as Effective Genetic Counselling for Presymptomatic Testing in Late-Onset Disorders? A Study of the Consultand’s Perspective
42. Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature
43. The use of genealogy databases for risk assessment in genetic health service: a systematic review
44. A study of the practice of individual genetic counsellors and genetic nurses in Europe
45. Development of an Evidence-Based Information Booklet to Support Parents of Children Without a Diagnosis
46. The Department of Health-supported genetic counsellor training post scheme in England: a unique initiative?
47. Suggested components of the curriculum for nurses and midwives to enable them to develop essential knowledge and skills in genetics
48. Counseling Adolescents and the Challenges for Genetic Counselors
49. A profile of the genetic counsellor and genetic nurse profession in European countries
50. Can We Make Assumptions About the Psychosocial Impact of Living as a Carrier, Based on Studies Assessing the Effects of Carrier Testing?
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