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Self-management toolkit Mast Cell Action are delighted to be able to share their self-management resource,...

 Learning Resources / 379 views

In-depth characterisation of a cohort of individuals with missense and loss-of- function variants disrupting FOXP2...

 Learning Resources / 452 views

Clinical Pearls: An interactive body map to help you manage the complexities associated with FOP,...

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This module provides an overview of genetic haemochromatosis, including the signs, symptoms, diagnosis, treatment, and...

 Learning Resources /  UK / 706 views / Popular

A brief description of Fragile X Syndrome: how it is caused, its effects, diagnostic tests,...

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Neurofibromatosis type 1 (NF1) is a genetic disorder with many and varied clinical manifestations, its...

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An immersive experience organised and funded by Kyowa Kirin to tell the stories of real people...

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The idea for AcroTales came about after a project co-ordinated by Dan Jeffries, Tessa Murdoch and...

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Neurofibromatosis type 1 (NF1) is a neurogenetic condition that approximately 1 in every 2,700 people...

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