| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Disclosure of Genetics Research Results after the Death of the Patient Participant: A Qualitative Study of the Impact on Relatives
|
Ormondroyd, E.
|
|
2007
|
16 |
4 |
p. 527-538
|
artikel
|
| 2 |
Health Beliefs and Behaviors of Women Who Have Received Genetic Counseling For Breast Cancer
|
Rees, Gwyneth
|
|
2007
|
16 |
4 |
p. 457-468
|
artikel
|
| 3 |
Information Processing in the Context of Genetic Risk: Implications for Genetic-Risk Communication
|
Etchegary, Holly
|
|
2007
|
16 |
4 |
p. 419-432
|
artikel
|
| 4 |
Knowledge and Attitudes Towards Genetic Testing: A Two Year Follow-Up Study in Patients with Asthma, Diabetes Mellitus and Cardiovascular Disease
|
Calsbeek, Hiske
|
|
2007
|
16 |
4 |
p. 493-504
|
artikel
|
| 5 |
Knowledge and Expectations of Women Undergoing Cancer Genetic Risk Assessment: A Qualitative Analysis of Free-Text Questionnaire Comments
|
Phelps, C.
|
|
2007
|
16 |
4 |
p. 505-514
|
artikel
|
| 6 |
Neurofibromatosis Type 1 in Genetic Counseling Practice: Recommendations of the National Society of Genetic Counselors
|
Radtke, Heather B.
|
|
2007
|
16 |
4 |
p. 387-407
|
artikel
|
| 7 |
Parents’ Perceptions of Functioning in Families Having a Child with a Genetic Condition
|
Knafl, Kathleen A.
|
|
2007
|
16 |
4 |
p. 481-492
|
artikel
|
| 8 |
Psychological Follow-up of Presymptomatic Genetic Testing for Spinocerebellar Ataxia Type 2 (SCA2) in Cuba
|
Paneque, Milena
|
|
2007
|
16 |
4 |
p. 469-479
|
artikel
|
| 9 |
Results of an Intervention for Individuals and Families with BRCA Mutations: A Model for Providing Medical Updates and Psychosocial Support Following Genetic Testing
|
McKinnon, Wendy
|
|
2007
|
16 |
4 |
p. 433-456
|
artikel
|
| 10 |
Risky Communication: Pitfalls in Counseling About Risk, and How to Avoid Them
|
O’Doherty, K.
|
|
2007
|
16 |
4 |
p. 409-417
|
artikel
|
| 11 |
Successful Use of Peer Educators for Sharing Genetic Information
|
Venne, Vickie L.
|
|
2007
|
16 |
4 |
p. 515-525
|
artikel
|
| 12 |
What do Patients Prefer: Informed Consent Models for Genetic Carrier Testing
|
Ormond, K. E.
|
|
2007
|
16 |
4 |
p. 539-550
|
artikel
|
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