A 12,000-Year-Old Case of NPR2-Related Acromesomelic Dysplasia | NEJM
Rare disease in an adolescent who lived more than 12,000 years ago, along with her burial embrace by a first-degree relative, may reflect the importance of care for survival. Ancient DNA analysis l...
Ancient DNA techniques make the earliest genetic diagnosis in an anatomically modern human who lived over 12,000 years ago.
Read the full publication for more details: www.nejm.org/doi/full/10....
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A great result from a great collaboration!!
09.07.2025 21:17 โ ๐ 2 ๐ 0 ๐ฌ 0 ๐ 0
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The WEATHER Project team are developing a new early weather warning system (EWS) for communities in the Durban area of South Africa where extreme weather events (EWEs) is leading to flash flooding.
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RDI is the global alliance for persons living with a rare disease, across all countries and all rare conditions.
An alliance of non-profit organisations working across borders and diseases to improve the lives of all people living with rare diseases.
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RDND Lab at Kingโs College London led by Cristina Dias. Clinical Geneticist and Rare Disease researcher. Rare Conditions, neurodevelopmental disorders of chromatin regulation and chromatin remodeller-TF interactions.
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The Max Planck Institute for Molecular Genetics in Berlin. We want to understand how the genome works and how it is regulated, especially during embryonic development & disease. Imprint: https://www.molgen.mpg.de/impressum
How do cells form tissues? Our research program spans the scales from molecules to organisms. News from the Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG) in Dresden, Germany. Impressum: https://www.mpi-cbg.de/impressum
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