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‘Morning people’ have lower breast cancer risk bbc.co.uk/news/health-46…

Outrageous!

nature.com/articles/s4158…

When you hear hoofbeats, sometimes it is Zebras! #RareDiseaseDay2021

Happy Mother’s Day

Did you know that there are over 6000 identified rare diseases around the world according to the European Journal of Human Genetics? Find out more about rare diseases on our website: cutt.ly/1RepKBP

It's #RareDiseaseDay! Today is all about raising awareness and generating change for the 300 million people worldwide living with a rare condition, their families and carers. Keep an eye out on our feeds throughout the day – Genetic Alliance UK Rare Disease UK #CareForRare

Today is Rare Disease Day and it’s a day to raise awareness for the 300 Million people in the world with over 6000 rare diseases. If you or a loved one have a rare disease write it in the comments and make it seen. #RareDisease #RareDiseaseDay #RareDiseaseDay2023

None of us want to strike 📈#medschool *debt*= £90-150,000 📈personal *cost* of training= £25-100,000 📉our salary 📈 mental/physical trauma from infantilisation, no respect & pandemic= priceless time to pay #juniordoctors what we’re worth #JuniorDoctorsStrike #medtwitter

Congratulations to all the British Society for Surgery of the Hand Hand Diploma Graduates of 2022. The Graduates at #BSSHSpring23 were presented with their certificates today 👏

Very interesting debate on genomic newborn screening, chaired by the excellent A/Prof Danya Vears. Are we ready yet? Half the audience said no before the debate, will the discussion change minds? #ESHG2023

Personal highlight Day 2 #ESHG2023 : Kristina Ibañez showing that neurological repeat expansion disorders may be *10* times more prevalent than thought!

It was so nice to hear from Julian G Barwell invaluable insight re UK perspectives and great work on population genomics.

At the UHL Recognition awards with the brilliant Research Space team short-listed for our Fragile X Syndrome work and the awe inspiring Dr Neeta Lakhani - the next big thing in genomic medicine, celebrating a well-deserved patient award nomination.

A team of UHL clinicians led by Clinical Geneticist, Dr Neeta Lakhani, have authored a new book to support clinicians when diagnosing and treating genetic conditions. Neeta said: “We are incredibly proud to get this project over the line & thank our expert who made it happen.”

So excited to see our book for children aged 8-12 explainng the role of DNA and how all living things are connected. Silly, entertaining but covering topics from evolution, through inheritance, mitochondria and behaviour without simplifying the content.Neeta Kulkarni

GP's are resorting to using pen and paper, as a GP's handwriting is the most secure encryption method known to mankind.. #nhscyberattack

NHS is in meltdown after a ransomware cyber attack earlier today #NHScyberattack

Tonight, 10.35pm, Channel 4...