Neurofibromatosis type 1 (NF1) is a neurogenetic condition that approximately 1 in every 2,700 people...
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An immersive experience organised and funded by Kyowa Kirin to tell the stories of real people...
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Neurofibromatosis type 1 (NF1) is a genetic disorder with many and varied clinical manifestations, its...
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Self-management toolkit Mast Cell Action are delighted to be able to share their self-management resource,...
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In-depth characterisation of a cohort of individuals with missense and loss-of- function variants disrupting FOXP2...
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This module provides an overview of genetic haemochromatosis, including the signs, symptoms, diagnosis, treatment, and...
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A brief description of Fragile X Syndrome: how it is caused, its effects, diagnostic tests,...
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Clinical Pearls: An interactive body map to help you manage the complexities associated with FOP,...
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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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