Useful Links

• Antenatal Results and Choices is a charity for parents wanting information and support on all aspects of antenatal screening. The charity is member of the PAGE consortium; their website provides a wealth of information and many useful links.
• Healthtalk Online: Personal experiences of antenatal screening, including decision-making after a prenatal diagnosis.
• Contact a Family: Information, support and advice for families with a child with any disability or special need, including expectant parents with a prenatal diagnosis. Information about a wide range of conditions, including rare conditions.
• Unique is a UK-based charity that provides information and support to families and individuals affected by any rare genetic disorder.
• Syndromes Without A Name is a project run by Genetic Alliance UK offering support and information to families of children with undiagnosed conditions.
• Genetic Alliance UK is the national charity of patient organisations supporting all those affected by genetic disorders.

• Genetic and Rare Disorders Organisation is a non governmental organisation based in Ireland acting as a national alliance for voluntary groups representing the views and concerns of people affected by or at risk of developing genetic or other rare disorders.
• Wellcome Trust Sanger Institute is a charitably funded genomic research institute which focuses on understanding the role of genetics in health and disease.
• yourgenome.org is a website intended to help people understand genetics and genomic science plus the implications for us all.
• insideDNA.org is a website on the latest developments in the fast-moving world of human genomics.
• Genomics England is a flagship project set up by the Department of Health to deliver 100,000 whole genomes from NHS patients by 2017. Initially the focus will be on rare disease, cancer and infectious disease.