Genomics England
@GenomicsEngland
We’re working to enable faster and deeper genomic research, to bring genomic healthcare to all who need it.
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http://www.genomicsengland.co.uk 28-06-2013 08:58:18
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📣 Help us reach more families this Undiagnosed Children's Day by sharing our reel! 📣 SWAN UK (syndromes without a name) is the only dedicated community for UK based families of children aged 0-25 years old who are searching for a genetic diagnosis. #UCD2024 #SyndromeWithoutAName ow.ly/CCLT50RoLoA
Each year, around 6,000 children are born in the UK with a genetic condition that will likely remain undiagnosed.
Today on Undiagnosed Children's Day, we're highlighting SWAN UK (syndromes without a name), a support community for families affected by a syndrome without a name.
ow.ly/wgKu50RfYMa
Today is National DNA Day! We're revisiting our podcast episode with Dr Francis Collins, co-leader of the landmark Human Genome Project, where he discussed his journey, and his thoughts on what's next in the world of genomics 🧬
Listen here: ow.ly/xpoC50QLOZw
#DNADay2024
It's Undiagnosed Children's Day on 26 April. Check out our previous podcast on the impact of 'no primary findings' results from genomic tests and the role of hope🎙️
Listen here: ow.ly/4gHI50ReQEs
Jana Gurasashvili Louise Fish Celine Lewis defnotthewaltons 💙 🇯🇪🇺🇦✡️ SWAN UK (syndromes without a name)
UK Research opportunity! Does your child have one of the genetic conditions listed here? Take part in the GenROC study to expand information resources that may help to provide better care for patients and their families. Scan the QR code or email [email protected]
Do you now someone with a child that has an undiagnosed condition?
Let them know about SWAN UK (syndromes without a name) - a community, run by Genetic Alliance UK, of support for families with children living with a syndrome without a name, or SWAN.
Amazing work by Nicky Whiffin and team including Yuyang Chen and Anne O'Donnell-Luria 🌟👏 This breakthrough is a great example of the power of new sequencing methods to uncover novel diagnoses for patients🧬