| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1089/GTMB.2008.0064 |
| P698 | PubMed publication ID | 19309267 |
| P50 | author | Christine Patch | Q38360082 |
| Joanna Picot | Q42662148 | ||
| William Rosenberg | Q50954381 | ||
| P2093 | author name string | Jackie Bryant | |
| Keith Cooper | |||
| Paul Roderick | |||
| Andy Clegg | |||
| P433 | issue | 1 | |
| P921 | main subject | systematic review | Q1504425 |
| P304 | page(s) | 7-14 | |
| P577 | publication date | 2009-02-01 | |
| P1433 | published in | Genetic Testing and Molecular Biomarkers | Q15753742 |
| P1476 | title | Psychosocial aspects of DNA testing for hereditary hemochromatosis in at-risk individuals: a systematic review | |
| P478 | volume | 13 |
| Q35143295 | A new approach to assessing affect and the emotional implications of personal genomic testing for common disease risk |
| Q38132275 | Diagnosis and treatment of hereditary hemochromatosis: an update |
| Q22330767 | Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders |
| Q39124510 | Parents' attitudes toward genetic testing of children for health conditions: A systematic review. |
| Q34173696 | Striking a balance in communicating pharmacogenetic test results: promoting comprehension and minimizing adverse psychological and behavioral response |
| Q37790364 | Systematic Review of Psychosocial Benefits and Harms of Genetic Testing |
| Q34113976 | The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop |
| Q37356785 | The global burden of iron overload |
| Q33534345 | The promise and challenges of incorporating genetic data into longitudinal social science surveys and research |
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