Experiences of predictive testing in young people at risk of Huntington's disease, familial cardiomyopathy or hereditary breast and ovarian cancer.
| Autor: | MacLeod, Rhona1, Beach, Anna1, Henriques, Sasha1, Knopp, Jasmin2, Nelson, Katie1, Kerzin-Storrar, Lauren1 |
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| Zdroj: | European Journal of Human Genetics. Mar2014, Vol. 22 Issue 3, p396-401. 6p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
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