Close
4th-6th September 2019

Join us at the 22nd SSBP International Research Symposium in Birmingham, UK.

Education Day

4th September 2019

Research Symposium

5th - 6th September 2019

Registration information will be available shortly. 

Please check back soon.

Online Abstract Submission

Extended Deadline 3rd May 2019

Early Bird Registrations

Discounted tickets available till 26th July 2019

Latest News and Information

Publicity materials for SSBP 2019 conference are now available.

Please click below to download a copy of the SSBP 2019 poster.

Please click below to download a copy of the SSBP 2019 postcard

honey

A message from the Chair of the SSBP

Welcome to the website of the Society for the Study of Behavioural Phenotypes (SSBP). The SSBP believes that progress in understanding the behavioural features associated with often complex genetic conditions is best served by providing a focus and point of contact for medical researchers and health care professionals working with those whose lives are affected by these conditions.

 

On our website and the linked SSBP Conference website you will find information about a wide range of syndromes and about the activities of the SSBP including our annual international research symposium, with its associated Education Days reaching out to the wider community of patients and their families.

 

Honey Heussler

SSBP Chair

 

The Society for the
Study of Behavioural Phenotypes (SSBP)

Siena Conference, Italy 2016

Our Affiliated Member Societies

The SSBP is proud to be affiliated with these member societies.
Fragile-X-Soc-Logo.png

Fragile X Society

Fragile X Syndrome is the most common inherited cause of learning disability. The Fragile X Society provides information and practical guidance to support and empower individuals and families living with Fragile X, and the professionals who support them. We also support research in order to improve support and understanding of all aspects of Fragile X.

MaxAppeal-Logo.png

Max Appeal

Max Appeal’s mission is to enable people with 22q11 syndromes to lead an independent and economically prosperous life as possible with Max Appeal being the voice to achieve appropriate medical care, social support, employment and empowerment for individuals and their families.