16p11.2 Duplication project
Thank you for your interest in my PhD project! Here are some links you may find relevant. You can also to email me, connect on LinkedIn or follow me on Bluesky!
Email
Email
LinkedIn
LinkedIn
Bluesky
Bluesky
Unique | Understanding Rare Chromosome and Gene Disorders
Unique | Understanding Rare Chromosome and Gene Disorders
3Rs of Animal Research in the UK
3Rs of Animal Research in the UK
Pioneering better science. Replacement, Reduction and Refinement. A UK-based scientific organisation dedicated to helping the research community worldwide to identify, develop and use 3Rs technologies and approaches.
What are copy number variants? - Genomics Education Programme
What are copy number variants? - Genomics Education Programme
16p11.2 - Academic Review Article
16p11.2 - Academic Review Article
Copy number variations (CNVs) of the human 16p11.2 genetic locus are associated with a range of neurodevelopmental disorders, including autism spectrum disorder, intellectual disability and epilepsy. In this review, we delineate genetic information ...
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