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Your search keyword '"Academic Centre on Rare Diseases (ACoRD)"' showing total 9 results

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9 results on '"Academic Centre on Rare Diseases (ACoRD)"'

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1. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

2. Analysis of shared heritability in common disorders of the brain

3. Efficacy and safety of regorafenib compared to placebo and to post-cross-over regorafenib in advanced non-adipocytic soft tissue sarcoma

4. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

5. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

6. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

7. Individual common variants exert weak effects on the risk for autism spectrum disorderspi

8. A genome-wide scan for common alleles affecting risk for autism

9. Wide disparity of clinical genetics services and EU rare disease research funding across Europe.

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