Category Archives: Policy

Mitochondrial disease – so what are the next steps?

Last week you couldn’t move for discussion and speculation about the debate of the draft Human Fertilisation and Embryology (Mitochondrial Donation) Regulations that was about to take place in the House of Commons. The media was full of ‘3 parent … Continue reading

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Cancer Genomes – Is sequencing or functional analysis the way forward?

An interesting article in this weeks Nature News looks at the completion of the multi-million dollar Cancer Genome Atlas project and considers which direction future work might take. With nearly 10 million cancer-related mutations identified, data from this project has … Continue reading

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Criticism over NHS Down’s syndrome test availability

According to BBC new, a new screening test for Down’s syndrome is still not available across the Welsh NHS, six years after guidelines said it should be. In 2008 the National Institute for Health and Care Excellence (NICE) said all … Continue reading

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New national competences follow in the footsteps of GPU’s work

We are delighted to see the launch of the Core competences in genetics for sickle cell and thalassaemia counselling. The work undertaken by the NHS Sickle Cell & Thalassaemia Screening Programme has been ongoing since Dec 2011 and Maggie Kirk … Continue reading

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Born Healthy – reducing the burden of birth defects in developing countries

The Born Healthy programme was established by the PHG Foundation as a response to the urgent need to reduce the burden of birth defects in developing countries. It has recently been singled out in a WHO report as one of … Continue reading

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