| Translational research policies: disruptions and continuities in biomedical innovation systems in Austria, Finland and Germany |
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| Attitudes of health care professionals toward carrier screening for cystic fibrosis. A review of the literature |
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| Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to consider |
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| Definitions of genetic testing in Italian legal documents |
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| Epidemiological profile of common haemoglobinopathies in Arab countries |
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| Consanguinity, endogamy, and genetic disorders in Tunisia |
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| The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users |
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| Conceptions on genetics in a group of college students |
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| Prenatal diagnosis and termination of pregnancy: perspectives of South African parents of children with Down syndrome |
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| Examining the family-centred approach to genetic testing and counselling among UK Pakistanis: a community perspective |
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| Genetics and public health: the experience of a reference center for diagnosis of 22q11.2 deletion in Brazil and suggestions for implementing genetic testing |
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| Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study |
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| Experiences of parents with a child with Down syndrome in Pakistan and their views on termination of pregnancy |
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| The challenge of implementing genetic tests with clinical utility while avoiding unsound applications |
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| Screening criteria: the need to deal with new developments and ethical issues in newborn metabolic screening |
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| The use of a Toolkit for health needs assessment on neural tube defects in Argentina |
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| Screening for the sickle cell gene in Gujarat, India: a village-based model |
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| A study of the practice of individual genetic counsellors and genetic nurses in Europe |
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| Erratum to: Perceptions of genetic research in three rural Appalachian Ohio communities |
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| Genetic risk |
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| Study of stillbirth and major congenital anomaly among newborns in the high-level natural radiation areas of Kerala, India |
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| Perceptions of genetic research in three rural Appalachian Ohio communities |
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| Genetics and democracy—what is the issue? |
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| Inclusion of medical genetics in primary health care: report of a pilot project in Brazil |
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| Genetic services and testing in the Philippines |
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| The family medical history as a tool in preconception consultation |
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| The use of genealogy databases for risk assessment in genetic health service: a systematic review |
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| Issues concerning the evaluation and regulation of predictive genetic testing |
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| Erratum to: Genetic services and testing in Brazil |
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| What can be offered to couples at (possibly) increased genetic risk? |
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| Preconception exposure to mutagens: medical and other exposures to radiation and chemicals |
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| Editorial: genetic aspects of preconception consultation in primary care |
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| Genetic services and testing in South Africa |
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| The Department of Health-supported genetic counsellor training post scheme in England: a unique initiative? |
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| Public–private partnership as a solution for integrating genetic services into health care of countries with low and middle incomes |
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| Psychosocial aspects of preconception consultation in primary care: lessons from our experience in clinical genetics |
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| Perceived familiarity with and importance of family health history among a medically underserved population |
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| Suggested components of the curriculum for nurses and midwives to enable them to develop essential knowledge and skills in genetics |
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| Genetic services and testing in Brazil |
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| Genetic testing and services in Argentina |
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| On the future of genetic risk assessment |
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| Neither as harmful as feared by critics nor as empowering as promised by providers: risk information offered direct to consumer by personal genomics companies |
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| Engaging African-Americans about biobanks and the return of research results |
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| Using a “genomics tool” to develop disease prevention strategy in a low-income setting: lessons from the podoconiosis research project |
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| Who is being referred to cancer genetic counseling? Characteristics of counselees and their referral |
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| Editorial: Genetics and Democracy |
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| Erratum to: How obedience of marriage rules may counteract genetic drift |
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| Genetics of autoimmune thyroid disease in the Lebanese population |
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| Upcoming special issues in the Journal of Community Genetics |
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| The wide variation of definitions of genetic testing in international recommendations, guidelines and reports |
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| Parental information use in the context of newborn bloodspot screening. An exploratory mixed methods study |
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| Earliest trace, so far, of community genetics as a distinct concept |
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| Revealing barriers and facilitators to use a new genetic test: comparison of three user involvement methods |
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| Are family-oriented interventions in Portuguese genetics services a remote possibility? Professionals’ views on a multifamily intervention for cancer susceptibility families |
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| Allelic clustering and ancestry-dependent frequencies of rs6232, rs6234, and rs6235 PCSK1 SNPs in a Northern Ontario population sample |
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| Genetic testing legislation in Western Europe—a fluctuating regulatory target |
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| Definitions of genetic testing in European legal documents |
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| Consolidating newborn screening efforts in the Asia Pacific region |
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