Latest papers

Pharmacogenetic testing: not as simple as it seems.

Genetic testing and primary care.

Community genetic services for congenital anomalies and genetic disorders in the Northwest of Iran.

Molecular genetic testing for ultra rare diseases: models for translation from the research laboratory to the CLIA-certified diagnostic laboratory.

Gene patenting and licensing: the role of academic researchers and advocacy groups.

Issues in genetic testing for ultra-rare diseases: background and introduction.

New quality assurance standards for rare disease testing.

The use by Alabama pediatricians of genetics consultation in the evaluation of developmental delay.

Cultural enhancement of a clinical service to meet the needs of indigenous people; genetic service development in response to issues for New Zealand Maori.

The genetics revolution and primary care pediatrics.

Ethical and legal issues in nutritional genomics.

[Are we threatened by misuse? Discreditation of medical genetics].

Outcome measurement in clinical genetics services: a systematic review of validated measures.

Tunisia: communities and community genetics.

Educational needs in genetic medicine: primary care perspectives.

Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarray.

Primary care physicians' concerns about offering a genetic test to tailor smoking cessation treatment.

Ethical and legal aspects of cancer genetic testing.

Practical aspects of delivering hereditary cancer risk counseling.

The Gulf Cooperation Countries genetic services. Understanding individuals, families, and community needs.