Extended Family Impact of Genetic Testing: The Experiences of X-linked Carrier Grandmothers
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://www.springerlink.com/index/pdf/10.1007/s10897-011-9360-2
Reference39 articles.
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2. Anido, A., Carlson, L. M., & Sherman, S. L. (2007). Attitudes toward fragile X mutation carrier testing from women identified in a general population survey. Journal of Genetic Counseling, 16, 97–104.
3. Armstrong, D., Michie, S., & Marteau, T. (1998). Revealed identity: a study of the process of genetic counselling. Social Science & Medicine, 47, 1653–1658.
4. Bailey, D. B., Skinner, D., Hatton, D., & Roberts, J. (2000). Family experiences and factors associated with the diagnosis of Fragile X Syndrome. Journal of Developmental and Behavioral Pediatrics, 21, 315–321.
5. Bailey, D. B., Jr., Sideris, J., Roberts, J., & Hatton, D. (2008). Child and genetic variables associated with maternal adaptation to fragile X syndrome: a multidimensional analysis. American Journal of Medical Genetics. Part A, 146A, 720–729.
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