| Confidence of primary care physicians in their ability to carry out basic medical genetic tasks—a European survey in five countries—Part 1 |
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| Challenges in recruiting Mexican women for cancer genetics research |
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| Erratum: A reply to community genetics: 1998–2009... and beyond |
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| Response to Dr. Zimmern |
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| Influence of genetic variants in the apolipoprotein A5 and C3 gene on lipids, lipoproteins, and its association with coronary artery disease in Indians |
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Indians |
| Development of a questionnaire for evaluating genetics education in general practice |
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| Points to consider in assessing and appraising predictive genetic tests |
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| A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka |
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| Using a community of practice to develop standards of practice and education for genetic counsellors in Europe |
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| Community genetics: 1998–2009…and beyond |
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| Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market |
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| Family matters: examining a multi-family group intervention for women with BRCA mutations in the scope of genetic counselling |
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| GenEthics and religion |
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| Prospective experience with contingent screening strategy for Down syndrome in Estonia |
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| A reply to community genetics: 1998–2009... and beyond |
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| Enhancing recruitment of African-American families into genetic research: lessons learned from Project SuGar |
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| Genetic diversity of hemoglobinopathies, G6PD deficiency, and ABO and Rhesus blood groups in two isolates of a primitive Kharia Tribe in Sundargarh District of Northwestern Orissa, India |
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Kharia Tribe |
| Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families |
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| ALOX5AP gene variants show differential association with coronary artery disease in different populations |
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| General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers’ practices |
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| Breast and ovarian cancer risk evaluation in families with a disease-causing mutation in BRCA1/2 |
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| Hereditary thrombophilic risk factors for recurrent pregnancy loss |
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| Updating and refining a study brochure for a cancer registry-based study of BRCA mutations among young African American breast cancer patients: lessons learned |
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| The importance and value of EQA for diagnostic genetic laboratories |
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| The journal of community genetics |
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| Assessing the risks and benefits of diagnosing genetic conditions with variable phenotypes through population screening: Klinefelter syndrome as an example |
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| Community genetics. Its definition 2010 |
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| Genetic variants at the APOE, lipoprotein lipase (LpL), cholesteryl ester transfer protein (CETP), and endothelial nitric oxide (eNOS) genes and coronary artery disease (CAD): CETP Taq1 B2B2 associate |
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Asian Indians |
| Scope of definitions of genetic testing: evidence from a EuroGentest survey |
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| Commentary: a sociologist's view on community genetics |
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| Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes |
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| How obedience of marriage rules may counteract genetic drift |
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