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BSHG is an independent body representing UK human genetics professionals. Its constituent organisations are:
 
·  Clinical Genetics Society (CGS)
·  Association for Clinical Cytogenetics (ACC)
·  Clinical Molecular Genetics Society (CMGS)
·  Association of Genetic Nurses and Counsellors (AGNC)
·  Cancer Genetics Group (CGG)
·  Society for Genomics, Policy and Population Health (SGPPH)
What's new
 
·

Clinical Genetics Society (CGS) Spring Conference 2013

14th March 2013

Brunei Gallery Lecture Theatre

School of Oriental and African Studies (SOAS)

University of London, Thornhaugh Street, Russell Square, London WC1N 0XG

REGISTRATION


Registration Closes Monday 4th March 2013 (09:00amGMT)



Association of Genetic Nurses and Counsellors Spring Meeting 2013

15th - 16th April 2013

Collingwood College, University of Durham, DURHAM

CALL FOR PAPERS

Abstract Submission Form

Closing date for receipt of abstracts: 11th February 2013 (17:00GMT)



Cancer Genetics Group Spring Conference 2013

22nd May 2013

The Queen’s Hotel, City Square Leeds, West Yorkshire LS1 1PJ

CALL FOR PAPERS

All abstracts MUST be submitted via the website

Closing date for receipt of abstracts: 11th February 2013




BSHG Annual Conference 2013

16-18 September 2013

Arena & Convention Centre, Liverpool


Cancer Genetics Group – Call for Papers, deadline 11th February 2013

Association of Genetic Nurses & Counsellors –  deadline 11th February 2013

Download call for papers

Download submission form


 

· NHS FASP: 18+0 to 20+6 weeks fetal anomaly scan: National standards and guidance for England

From Monday 2nd April to Monday 30th April 2012 the NHS Fetal Anomaly Screening Programme (FASP) will be undertaking an online consultation. The focus of this consultation will be reviewing the 18+0 to 20+6 weeks fetal anomaly scan: National standards and guidance for England.

- Consultation Feedback Form
- Consultation Letter
- 18+0 to 20+6 Weeks Fetal Anomaly Scan: National Standards and Guidance for England
- 18 to 20 weeks fetal anomaly ultrasound Consultation Flyer
 
· New advances prompt genetics guidance update

A new report from the Royal College of Physicians (RCP), Royal College of Pathologists and British Society for Human Genetics exploring benefits for diagnoses, risk prediction and clinical management, and accompanying ethical and legal issues of managing information that is relevant to both the individual and their family.

Consent and confidentiality in clinical genetic practice: Guidance on genetic testing and sharing genetic information
 
· Genetic Testing of Children
Report of a working party of the
British Society for Human Genetics

Guidelines
genetic testing children
· The British Society for Human Genetics is grateful for the opportunity to respond to the Public consultation on the revision of Directive 98/79/ec of the European Parliament and of the Council of 27 October 1998 on the IVD directive

Revision of European IVD directive response from the British Society for Human Genetics


Response from the European Society of Human Genetics


· Launch of HGC Principles for direct genetic tests - 4 August 2010

The Human Genetics Commission, the UK Government's advisory body on developments in genetics and their ethical, legal, social and economic implications, has launched today a 'Common Framework of Principles' for direct-to-consumer genetic testing services. A copy of the Principles can be downloaded here.

These Principles, which are applicable in different jurisdictions, have been developed in conjunction with representatives from the international genetic testing industry and represent a high level of consensus about what constitute good practice. They offer a guide to consumers, as well as service providers and regulators, about the elements that should make up a good quality direct genetic testing service.

 
· BSHG response to "Gene Tests: the new Russian roulette?" (Daily Mail, Tuesday May 25 2010)

The British Society for Human Genetics welcomes public discussion of the issues raised by genetic testing. Overall, this article provides a balanced overview of both the benefits of genetic testing, and the difficult decisions sometimes faced by families affected by genetic conditions. However, the BSHG is disappointed that a comment from the society about the future use of genetic testing in healthcare - for example to predict response to certain medicines - was cut short and taken out of context. The article further suggests that genetic tests may one day be used to routinely check embryos and prospective parents for genetic changes that cause disease. The BSHG would like to clarify that it does not share this view, and that the decision to take a genetic test should always remain with the individuals and families concerned.

 

· ELECTRONIC COMMUNICATION - No more paper copies - ALL information to members will now be ELECTRONIC. This will greatly benefit everyone

- the Society from incurring large printing and postage costs

- members will be able to access and store the information more quickly and efficiently

- helping the environment.

Please ensure that the Administrative Office ([email protected]) has your up to date EMAIL address


 BSHG response to the HGC consultation
on a framework of Principles for Direct to
Consumer Genetic Testing

 

· HGC consultation

see details

 

· Genetics Committee of National Institute for Health Research
see details
 
 
· A joint response to the Ministry of Justice consultation paper on the use and sharing of personal information in the public and private sectors
 
· Response to the consultation by the Association of British Insurers on their
Code of Practice for Genetic Tests

 
· Response to the draft Guidelines on Human Biobanks and Genetic Research Databases
 
· House of Lords Science and Technology Committee
Call for evidence: Genomic Medicine

A response from the British Society for Human Genetics
 
   
· Data Sharing Review- A response by the BSHG and JCMG
   
·
ITV1 programme - 'The killer within' BSHG complaints

OFCOM

ITV1

OFCOM response to the British Society for Human Genetics

   
· ORPHANET is a database dedicated to information on rare diseases and orphan drugs. Access to this database is free of charge. Sign up here
   
· New title published by the Royal College of Physicians - The Science of Morality
   
· JCMG Guidance  on The Human Tissue Act-Amended version
   
· Consent and confidentiality in genetic practice - A report of the joint committee on medical genetics Report Contents
 
 
   
· Promoting Equity of Access to Genetic Healthcare-a report by the Genetic Interest Group
   
· Do Once and Share Clinical Genetics- Final Report.
   
· RCP seeking volunteers for Invited Service Reviews team members.
   
    Book Club
· Scion Publishing - 20% discount for BSHG members
· Oxford University press. 20% discount for BSHG members

 

 

 

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