Genetic testing, governance, and the family in the People's Republic of China.

Huntington's disease.

Commission agrees framework to regulate genetic tests sold direct to consumers.

Counterpoint: implementing population genetic screening for Lynch Syndrome among newly diagnosed colorectal cancer patients--will the ends justify the means?

Ashkenazi Jewish screening in the twenty-first century.

Genotype of lattice corneal dystrophy (R124C mutation in TGFBI) in a patient presenting with features of avellino corneal dystrophy.

[The importance of quality assurance in molecular genetic laboratories]

Consent to 'personal' genomics and privacy. Direct-to-consumer genetic tests and population genome research challenge traditional notions of privacy and consent.

Antenatal screening for haemoglobinopathies in primary care: a cohort study and cluster randomised trial to inform a simulation model. The Screening for Haemoglobinopathies in First Trimester (SHIFT) trial.

Non-invasive prenatal diagnosis using cell-free fetal DNA technology: applications and implications.

Clinical and ethical considerations in pharmacogenetic testing: views of physicians in 3 "early adopting" departments of psychiatry.

You are born with your genes: justice and protection against discrimination in the use of genetic information.

[Neonatal screening--more hidden compulsion?]

A survey of the knowledge and attitudes of pregnant Thai women towards Down syndrome screening.

Facilitating informed decisions regarding microsatellite instability testing among high-risk individuals diagnosed with colorectal cancer.

Ethical challenges in providing noninvasive prenatal diagnosis.

American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.

Ethical considerations in mental health care informed by research.

[Practical genetic counseling and testing in clinical neurology]

ERCC2, ERCC1 polymorphisms and haplotypes, cooking oil fume and lung adenocarcinoma risk in Chinese non-smoking females.

Direct-to-consumer genomics and research ethics: should a more robust informed consent process be included?

Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how?

Ethical, legal and social implications of prenatal and preimplantation genetic testing for cancer susceptibility.

Tumour tissue: who is in control?

Prenatal diagnosis and the trouble with eugenics.