Ausgabe 4/2007
Inhalt (12 Artikel)
Neurofibromatosis Type 1 in Genetic Counseling Practice: Recommendations of the National Society of Genetic Counselors
Heather B. Radtke, Courtney D. Sebold, Caroline Allison, Joy Larsen Haidle, Gretchen Schneider
Risky Communication: Pitfalls in Counseling About Risk, and How to Avoid Them
K. O’Doherty, G. K. Suthers
Information Processing in the Context of Genetic Risk: Implications for Genetic-Risk Communication
Holly Etchegary, Colin Perrier
Results of an Intervention for Individuals and Families with BRCA Mutations: A Model for Providing Medical Updates and Psychosocial Support Following Genetic Testing
Wendy McKinnon, Shelly Naud, Taka Ashikaga, Rose Colletti, Marie Wood
Health Beliefs and Behaviors of Women Who Have Received Genetic Counseling For Breast Cancer
Gwyneth Rees, Clara Gaff, Mary-Anne Young, Paul R. Martin
Psychological Follow-up of Presymptomatic Genetic Testing for Spinocerebellar Ataxia Type 2 (SCA2) in Cuba
Milena Paneque, Carolina Lemos, Karell Escalona, Lizandra Prieto, Rubén Reynaldo, Mercedes Velázquez, Judith Quevedo, Nieves Santos, Luis Enrique Almaguer, Luis Velázquez, Alda Sousa, Manuela Fleming, Jorge Sequeiros
Parents’ Perceptions of Functioning in Families Having a Child with a Genetic Condition
Kathleen A. Knafl, George J. Knafl, Agatha M. Gallo, Denise Angst
Knowledge and Attitudes Towards Genetic Testing: A Two Year Follow-Up Study in Patients with Asthma, Diabetes Mellitus and Cardiovascular Disease
Hiske Calsbeek, Mattijn Morren, Jozien Bensing, Mieke Rijken
Knowledge and Expectations of Women Undergoing Cancer Genetic Risk Assessment: A Qualitative Analysis of Free-Text Questionnaire Comments
C. Phelps, F. Wood, P. Bennett, K. Brain, J. Gray
Successful Use of Peer Educators for Sharing Genetic Information
Vickie L. Venne, Heidi A. Hamann
Disclosure of Genetics Research Results after the Death of the Patient Participant: A Qualitative Study of the Impact on Relatives
E. Ormondroyd, C. Moynihan, M. Watson, C. Foster, S. Davolls, A. Ardern-Jones, R. Eeles
What do Patients Prefer: Informed Consent Models for Genetic Carrier Testing
K. E. Ormond, M. Iris, S. Banuvar, J. Minogue, G. J. Annas, S. Elias