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The successful achievement of pregnancies following pre-implantation genetic diagnosis (PGD) was first reported in April 1990. The technology is often used for patients who are at substantial risk of conceiving a pregnancy affected by a known genetic disorder, however from this technology other more controversial uses have arisen such as HLA typing to save the life of a sibling, gender selection for social reasons, the prevention of late onset diseases, or the prevention of diseases which may be genetically predisposed to developing such as breast cancer. The technology surrounding PGD is constantly developing, giving rise to new and unexpected consequences that create fresh ethical and lega...
'Born and Made' examines the case of preimplantation genetic diagnosis (PGD), the procedure used to prevent serious genetic disease by embryo selection, and the so-called 'designer baby' method. It shows that far from being a runaway technology, the regulation of PGD provides an example of precaution and restraint.
In 2015 the UK became the first country in the world to legalise mitochondrial donation, a controversial germ line reproductive technology to prevent the transmission of mitochondrial disease. Dimond and Stephens track the intense period of scientific and ethical review, public consultation and parliamentary debates preceeding the decision. They draw on stakeholder accounts and public documents to explore how patients, professionals, institutions and publics mobilised within ‘for’ and ‘against’ clusters, engaging in extensive promissory, emotional, bureaucratic, ethical, embodied and clinical labour to justify competing visions of an ethical future. They describe how this decision is...
Unnatural acts by Robert Todd Carroll, creator of the popular website The Skeptic's Dictionary, is for people who want to improve their thinking, become more accurate in their beliefs and more reasonable in their actions, and who are tired of being fooled by others. The book is about natural and unnatural thinking, and how the way we think affects everything we do - Publisher's description.
The Novartis Foundation Series is a popular collection of the proceedings from Novartis Foundation Symposia, in which groups of leading scientists from a range of topics across biology, chemistry and medicine assembled to present papers and discuss results. The Novartis Foundation, originally known as the Ciba Foundation, is well known to scientists and clinicians around the world.
This book is based on the RCOG Study Group findings on reproductive ageing.
Presenting for the first time, in original detail, Drs Edwards and Steptoe's breakthroughs leading to the birth of Louise Brown.
Approximately 1% of births in the UK were conceived using IVF. At present IVF and embryo research are controlled by the Human Fertilisation and Embryology Authority which was formed by a 1990 Act, since then scientific progress has been rapid and the Department of Health has announced a review of that Act. This extensive inquiry will inform that review. It covers: regulation of assisted reproduction, problems with HFE Act; the operation of the Act; provision of infertility services; review of the Act; legislative and regulatory models. It makes recommendations on issues such as choosing the sex of babies; the need for a separate review of abortion; the regulatory bodies required; and a legislative framework that balances the freedom of the individual with the interests of the state, so that any intervention has a sound ethical base.
This is your source for authoritative and comprehensive guidance from the British Medical Association (BMA) Medical Ethics Department covering both routine and highly contentious medico-legal issues faced by health care professionals. The new edition updates the information from both the legal and ethical perspectives and reflects developments surrounding The Mental Capacity Act, Human Tissue Act, and revision of the Human Fertilisation and Embryology Act.
With genetic technologies advancing rapidly, Aisling de Paor examines the urgent need for an EU-level framework to regulate genetic information.