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2. Discovery of DNA methylation signature in the peripheral blood of individuals with history of antenatal exposure to valproic acid

5. Identification of a DNA methylation episignature for recurrent constellations of embryonic malformations

6. Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome

7. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

8. Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profiles

9. MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature

10. The Path to a Match for Interventional Cardiology Fellowship: A Major SCAI Initiative

11. Scalable Reverse Image Search Engine for NASAWorldview

14. Diagnostic utility and reporting recommendations for clinical DNA methylation episignature testing in genetically undiagnosed rare diseases

16. Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

17. DNA methylation episignature, extension of the clinical features, and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7

18. Identification of DNA methylation episignature for the intellectual developmental disorder, autosomal dominant 21 syndrome, caused by variants in the CTCF gene

20. Optimizing the location of vaccination sites to stop a zoonotic epidemic

21. Microduplications of ARID1A and ARID1B cause a novel clinical and epigenetic distinct BAFopathy

26. Clinico-biological refinement of BCL11B-related disorder and identification of an episignature: A series of 20 unreported individuals

28. Development of a Computer-aided Prediction Tool for Evaluating Brushing Samples of Biliary Strictures

29. Protocol for an Observational Study on the Effects of Social Distancing on Influenza-Like Illness and COVID-19

33. Identification of a robust DNA methylation signature for Fanconi anemia

38. DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder

47. Intracerebral Aneurysms

49. 36-month clinical outcomes of patients with venous thromboembolism: GARFIELD-VTE

50. Human microglia maturation is underpinned by specific gene regulatory networks

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