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Do you know someone seeking a diagnosis of a genetic or rare condition? The journey can be long, difficult and worrying. We hope our new resources can support every step of the way. Please help us share them far and wide. 👉 geneticalliance.org.uk/sard-children/ 👉 geneticalliance.org.uk/sard-adults/

Bethany Lumborg gives us an update on the GenPan Network and their achievements and development over the last two years 🧬 #AGNC2025 #genechat

Lauren Kerzin-Storrar Prize winner Louiza Irodotou speak to us about her MSc dissertation on GC and patient value conflicts, exploring GC experiences and impact 🧬🏆🎓#AGNC2025 #genechat

Principal GC and Chair of AGNC, Roberta Rizzo, talks us through the history and evolution of the AGNC ✨🌍 #AGNC2025 #genechat

Next we have a GTAC update from Heidy Brandon, Principal GC, and Laura Boyes, Consultant GC 🧬 really great to hear how far things have come since last year’s conference! Genomics Education NHS England #AGNC2025

Georgina Hall, Consultant GC, gives us an update on the GCRAB, routes of registration for GCs and how the GCRAB establishes and supports standards of practice in genetic counselling #AGNC2025 #genechat

A strong focus on Lynch syndrome today! Andrew Beggs Consultant Colorectal Surgeon at University Hospitals Birmingham gives us an in-depth review of advances in Lynch syndrome management and research #AGNC2025 #genechat

Moving from paediatric to adult services can be daunting for young people with polyposis syndromes. Dr Ronald Bremner, Consultant Paediatric Gastroenterologist, tells us how they do things at the Polyposis Transition Clinic at Bham Children's Hosp 💙 #AGNC2025 #genechat

Research GC, Jonathan Robert’s asks what do people want from a genetic counselling research network? #AGNC2025 #genechat

Brilliant lightning talk from Amy Braddel giving their experience of establishing a regional MND genetic testing care pathway #AGNC2025 #genechat

A problem lots of GCs and family history nurses face - how do you assess cancer risk for patients with an unconfirmed family history? Jamey Thom tells us about the experience at University Hospital Southampton 💙 #AGNC2025 #genechat

It’s always great to hear from Unique Thank you Francesca Wicks for your talk on living with a rare chromosome or gene disorder and what actions GCs and nurses can take to support these families 🧬#AGNC2025 #genechat

And finally!! Shaun Griffin, GC at St George's, Epsom and St Helier, tells us about the impact of public and patient involvement in Clinical Genomics research #AGNC2025 #genechat

#AGNC2025 meeting in Birmingham was fantastic! It was wonderful to connect with many colleagues in person. A huge thank you to the AGNC committee, the Birmingham team, and everyone who put in the effort to organize such a successful event Roberta Rizzo CatherineMWatt gcnotes

First speaker of the session joins us virtually Anneke Lucassen to introduce ethical principles in Genomic medicine #ESHG #precisionmedicine

Life with Williams Syndrome is more than you can imagine... By Liz Martin – Williams syndrome If you'd like to learn more about Williams syndrome or access support you can find more information with, Williams Syndrome UK.

Happy #DNAday 🧬!

Happy World Pilots' Day to all the legendary voices from the cockpit. 👨‍✈️✈👩‍✈️ Sometimes a little hard to understand but always full of heart and passion, guiding us safely through the skies. #flyswiss #flyswisscrew #worldpilotsday

WEBINAR Sácale el Máximo Provecho al Panel de Portadores 🗣️ luisalcaraz 📅 21/5- 30'- Español Hora local de cada país 20_00 España 12:00 México | Guatemala 13:00 Colombia | Ecuador | Perú 14:00 Chile | Rep. Dominicana | Venezuela 15:00 Uruguay 🔗 buff.ly/REj2t5H

#ESHG2025 Lovely talk from Dr. Susan Treves exploring how we identify and assess RYR1 variants, and use experimental tools to resolve variants of uncertain significance (VUS) in RYR1-related muscle disorders. #Neuromuscular #Genetics #RYR1