Disclosure of Genetic Research Results to Members of a Founder Population-Reference-Cited by-同舟云学术

Disclosure of Genetic Research Results to Members of a Founder Population

Published:2014-04-29 Issue:6 Volume:23 Page:984-991
ISSN:1059-7700
Container-title:Journal of Genetic Counseling
language:en
Short-container-title:J Genet Counsel

Author:

Anderson Rebecca L.,Murray Kathleen,Chong Jessica X.,Ouwenga Rebecca,Antillon Marina,Chen Peixian,Diaz de Leon Lorena,Swoboda Kathryn J.,Lester Lucille A.,Das Soma,Ober Carole,Waggoner Darrel J.

Publisher

Wiley

Subject

Genetics(clinical)

Link

http://link.springer.com/content/pdf/10.1007/s10897-014-9721-8

Reference34 articles.

1. Armistead, J., Khatkar, S., Meyer, B., Mark, B. L., Patel, N., Coghlan, G., et al. (2009). Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome. [Comparative Study Research Support, Non-U.S. Gov’t]. American Journal of Human Genetics, 84(6), 728–739. doi: 10.1016/j.ajhg.2009.04.017 .

2. Beaulieu, C. L., Huang, L., Innes, A. M., Akimenko, M. A., Puffenberger, E. G., Schwartz, C., et al. (2013). Intellectual disability associated with a homozygous missense mutation in THOC6. Orphanet Journal of Rare Diseases, 8(1), 62. doi: 10.1186/1750-1172-8-62 .

3. Beskow, L. M., & Burke, W. (2010). Offering individual genetic research results: context matters. [Research Support, N.I.H., Extramural]. Science Translational Medicine, 2(38), 38cm20. doi: 10.1126/scitranslmed.3000952 .

4. Beskow, L. M., Burke, W., Fullerton, S. M., & Sharp, R. R. (2012). Offering aggregate results to participants in genomic research: opportunities and challenges. Genetics in Medicine, 14(4), 490–496. doi: 10.1038/gim.2011.62 .

5. Bogershausen, N., Shahrzad, N., Chong, J. X., von Kleist-Retzow, J. C., Stanga, D., Li, Y., et al. (2013). Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability. American Journal of Human Genetics, 93(1), 181–190. doi: 10.1016/j.ajhg.2013.05.028 .

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