Résultat de recherche

Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension...

A new treatment discovered at Institut Imagine and developed by QED Therapeutics...

Discovery of a new genetic disease predisposing to mycobacterial infec...

Deep phenotyping unstructured data mining in an extensive pediatric database...

Improving a full-text search engine: the importance of negation detection...

Mortality and functional outcome after pediatric intracerebral hemorrhage:...

Deep phenotyping unstructured data mining in an extensive pediatric database...

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Bi-allelic pathogenic variations in DNAJB11 cause Ivemark II syndrome,...

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Disruption of pathways regulated by Integrator complex in Galloway-Mowat...

Integrative genetic and immune cell analysis of plasma proteins in healthy...

CNVxplorer: a web tool to assist clinical interpretation of CNVs in rare...

Cell-ID: gene signature extraction and cell identity recognition at individual...

Primary immunodeficiencies suggest redundancy within the human immune ...

Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative...

MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hyp...

Mosaic Heterochrony in Neural Progenitors Sustains Accelerated Brain Growth...

Disruption of POGZ Is Associated with Intellectual Disability and Autism...