Medical Genetics Section

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Medical Genetics 2018/2019 dates for your diary

 

28-Nov-18 Diagnostic challenges and clinical management of DNA repair disorders - book now

20-Feb-19 The unusual suspects: Rare diseases in everyday medical care - book now

12-Jun-19 Epigenetics

 

For more information on the events that are not available online yet, or to book your place, please contact our customer service team on:

Tel: 02072 903 941

Email: events@rsm.ac.uk

About this section

Purpose:

To facilitate cross-specialty education, integration and progress in the field of genetic medicine and to provide insight into and promote recent advances in genetic medicine as a cross-cutting discipline. 

Section members:

Clinical geneticists, neurologists, rheumatologists. 

Section council:

Section meetings and conferences are usually organised by members of the Section council, led by the Section President.

events listing

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The unusual suspects: Rare diseases in everyday medical care
The unusual suspects: Rare diseases in everyday medical care

Wednesday 20 February 2019, Royal Society of Medicine
1 Wimpole Street
LONDON
W1G 0AE

Explore how generalists can approach patients with rare diseases, and become advocates for them. Hear a real patient experiences, and learn about the role genomics plays in everyday medicine. 

Half Day | Registration: 12:30 | Organised by: Medical Genetics Section, Medics 4 Rare Diseases |
Region: | Accreditation: CPD - Applied for Find out more Arrow Links

Online learning

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Visit RSM videos to view recently recorded lectures relevant to this Section

previous meetings More previous meetings

contact us

Medical Genetics Section
T: +44 (0)20 7290 3940

genetics@rsm.ac.uk arrow

Access medical genetics specialty e-journals

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Access over 5,000 full text e-journals as an RSM member including:

  • BMC Genomics
  • Case Reports in Genetics

 

Section Bibliography

For a list of what we have available via the library for this section, visit our bibliography page and then select the appropriate section link.