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2. Essential role for inflammatory signals in the differentiation and function of regulatory B cells

5. 'Good wood on crowdpleasers': humour publications in the Ming Wanli period

6. Large-scale discovery of novel genetic causes of developmental disorders

8. The Global Leadership Mentoring Community: building capacity across seven global regions

9. The Global Leadership Mentoring Community: building capacity across seven global regions

12. Identification of symbol digit modality test score extremes in Huntington's disease

13. Comprehensive cancer-predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes

14. Publisher Correction: Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

15. Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

18. Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disorders

19. Prevalence and architecture of de novo mutations in developmental disorders

20. Epidemiological and genetic considerations in retinoblastoma

21. Suicidal ideation in a European Huntington's disease population

25. A Municipal Hospital

33. The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients

34. Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY

35. Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY

36. Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

37. Phenotype and genotype in Nicolaides-Baraitser syndrome

38. Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism

39. Large-scale discovery of novel genetic causes of developmental disorders

40. Mutations in CDK5RAP2 cause Seckel syndrome

41. β-Defensin Genomic Copy Number Does Not Influence the Age of Onset in Huntington's Disease

42. Discrepancies in reporting the CAG repeat lengths for Huntington's disease

43. Encouraging role based online learning environments - The BLUE Report

45. Encouraging Role Based Online Learning Environments

46. Misconceptions

47. Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling

50. Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)

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