Ausgabe 4/2005
Inhalt (6 Artikel)
Genetic Counseling for Fragile X Syndrome: Updated Recommendations of the National Society of Genetic Counselors
Allyn McConkie-Rosell, Brenda Finucane, Amy Cronister, Liane Abrams, Robin L. Bennett, Barbara J. Pettersen
Policy Recommendations for Carrier Testing and Predictive Testing in Childhood: A Distinction That Makes a Real Difference
Susan Hogben, Paula Boddington
Educating Genetic Counselors in Australia: Developing an International Perspective
Margaret A. Sahhar, Mary-Anne Young, Leslie J. Sheffield, MaryAnne Aitken
Women’s Attitudes Toward Testing for Fragile X Carrier Status: A Qualitative Analysis
Aimee Anido, Lisa M Carlson, Lisa Taft, Stephanie L. Sherman
Psychosocial Issues That Face Patients With Charcot-Marie-Tooth Disease: The Role of Genetic Counseling
Angela Arnold, Meriel McEntagart, David S. Younger
An Assessment of Risk Understanding in Hispanic Genetic Counseling Patients
Jennifer N. Eichmeyer, Hope Northrup, Michael A. Assel, Thomas J. Goka, Dennis A. Johnston, Aimee Tucker Williams