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1. Genomic architecture of autism from comprehensive whole-genome sequence annotation.

2. What Does Competency Have to Do with It? Ethics Fellowship Training and the Experience of a Hospital-Based Program in Canada

5. Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation

6. New Developments and Old Dilemmas in Ontario’s Resuscitation Policy at the End of Life.

7. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

9. “Not Until the Baby Arrives”: When Delusional Pregnancy Impacts the Management of Uterine Cancer.

10. The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants

12. Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

13. Ethics Debriefs and Moral Distress: What are we Doing?

14. A national look at the influence of accreditation on Medical Council of Canada Qualifying Examination (MCCQE Part I) scores

19. Impact of DNA source on genetic variant detection from human whole-genome sequencing data

20. Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation

23. Generalization of DNA microarray dispersion properties: microarray equivalent of t-distribution

24. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

25. Overexpression of human CRB1 or related isoforms, CRB2 and CRB3, does not regulate the human presenilin complex in culture cells

26. Whole Genome Sequencing as a Genetic Test for Autism Spectrum Disorder: From Bench to Bedside and then Back Again

27. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

28. Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations

29. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

30. Difficult healthcare transitions

31. Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine

32. MG-108 Beyond the ACMG 56: Parental choices and initial results from a comprehensive whole genome sequencing-based search for predictive genomic variants in children

33. MG-132 Diagnostic utility of whole genome sequencing in paediatric medicine

34. Generalization of DNA microarray dispersion properties: microarray equivalent of t-distribution

35. Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome

37. Reflections on the Cost of 'Low-Cost' Whole Genome Sequencing: Framing the Health Policy Debate

38. Reflections on the Cost of "Low-Cost" Whole Genome Sequencing: Framing the Health Policy Debate

41. Generalization of DNA microarray dispersion properties: microarray equivalent of t-distribution

44. Ex-ad-geration

45. Moving beyond reach

46. A road map for retail marketers

47. Measuring What Matters.

48. Difficult healthcare transitions: Ethical analysis and policy recommendations for unrepresented patients.

49. Whole Genome Sequencing as a Genetic Test for Autism Spectrum Disorder: From Bench to Bedside and then Back Again.

50. Building trust in 21st century genomics.

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