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NEWS & EVENTS

  • 24th March 2020

    Coronavirus (COVID-19) advice for patients with rare genetic disorders

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  • 11th February 2020

    Rare Disease Day – 29th February, 2020

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  • 21st October 2019

    Strategy Vlog: Genomics

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Tweets by NWGLH

Other

(Manchester led studies)

Companion – Exploring Access to Genomic Research

Genetics of Stillbirth

(Externally led studies)

Dermatology Conditions ­- Study of a rare cutaneous lichenoid, alopecic and scarring variants

Genes and the Kidney in Tuberous Sclerosis – A study of natural history of renal disease in TSC2/PKD1 Contigious gene deletion syndrome

Immune Tolerance Induction with Methotrexate in Hurler Syndrome

INSIGNIA – Exploring the biological processes underlying mutational signatures identified in patients with inherited disorders and in patients exposed to mutagens

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Running late for an appointment? 0161 701 0254
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Paediatric Metabolic disorders: 0161 701 2137 (9am-5pm, Mon-Fri)
0161 276 1234 (out of hours)
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