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Your search keyword '"Tenconi, R"' showing total 423 results

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423 results on '"Tenconi, R"'

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1. Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature.

2. Selecting appropriate empirical antibiotic regimens for paediatric bloodstream infections: application of a Bayesian decision model to local and pooled antimicrobial resistance surveillance data

3. Variation in paediatric hospital antibiotic guidelines in Europe

5. Down Syndrome and Parity

7. SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

8. DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes

11. The worldwide Antibiotic Resistance and Prescribing in European Children (ARPEC) point prevalence survey: developing hospital-quality indicators of antibiotic prescribing for children

18. Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide

19. Selecting appropriate empirical antibiotic regimens for paediatric bloodstream infections: application of a Bayesian decision model to local and pooled antimicrobial resistance surveillance data

20. Variation in paediatric hospital antibiotic guidelines in Europe

22. Selecting appropriate empirical antibiotic regimens for paediatric bloodstream infections: Application of a Bayesian decision model to local and pooled antimicrobial resistance surveillance data

23. Variation in paediatric hospital antibiotic guidelines in Europe

24. Antibiotic resistance prevalence in routine bloodstream isolates from children's hospitals varies substantially from adult surveillance data in Europe

28. SHOX region mutation in Leri-Weill dischondrosteosis (LWS)

31. Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative study

33. The antibiotic resistance and prescribing in European Children project: a neonatal and pediatric antimicrobial web-based point prevalence survey in 73 hospitals worldwide

35. Pathophysiology, favoring factors, and associated disorders in otorhinosinusology

36. Peritoneal tuberculosis due to multidrug-resistant Mycobacterium tuberculosis

37. SHOX region mutation in Leri-Weil dischondrosteosis (LWS)

38. N-myristoylation of SHOC2 affects human development and growth

39. The +61 A-G polymorphism of the epidermal growth factor gene is not associated with occurrence of non-melanocytic skin tumors in transplant recipients

40. The italian XLMR bank: a clinical and molecular database

44. Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome

45. Down syndrome and parity

46. Paternal origin of LMNA mutations in Hutchinson-Gilford progeria [1]

47. Geographical and ethnic variation of the 677C > T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide: findings from over 7000 newborns from 16 areas world wide

48. Genomic imbalances in patients with a clinical presentation in the spectrum of Cornelia de Lange syndrome

49. La famiglia 'Williams'

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