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1. Chemoproteogenomic stratification of the missense variant cysteinome.

4. The Experience of Adults Recovering from an Eating Disorder in Professionally-Led Support Groups

6. Supports for university counselors impacted by student suicide: A systematic review and thematic synthesis.

9. Replication of the Learning Alliance Inventory to Blended Student Populations

11. Safety and efficacy of low-dose sirolimus in the PIK3CA-related overgrowth spectrum

12. Truck drivers are also lay rescuers: A scoping review.

13. Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland

14. Optimizing the Diagnosis of Rare Genomic Disease in the UK and Ireland

15. Optimising diagnostic yield in highly penetrant genomic disease

17. Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review

19. The Effect of Test-Taking Strategies on the Test Scores of Middle School Level Students.

22. Controlling Intramolecular Interactions in the Design of Selective, High-Affinity Ligands for the CREBBP Bromodomain

25. Somatic interventions therapists use when treating women presenting with sexual assault trauma involving tonic immobility.

28. Genetic testing for hereditary hyperparathyroidism and familial hypocalciuric hypercalcaemia in a large UK cohort

29. Contributors

30. Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD

33. Management of primary hyperparathyroidism in pregnancy: a case series

36. Bayesian approach to determining penetrance of pathogenic SDH variants

37. Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy

38. Bayesian approach to determining penetrance of pathogenic SDH variants

39. C2.2 Postzygotic activating variants in mapk pathway genes cause intracranial and extracranial vascular malformations that respond to targeted inhibition

40. SDHA related tumorigenesis: a new case series and literature review for variant interpretation and pathogenicity

41. Tumour risks and genotype–phenotype–proteotype analysis of patients with germline mutations in the succinate dehydrogenase subunit genes SDHB, SDHC, and SDHD

42. Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHCand SDHD

45. Bayesian approach to determining penetrance of pathogenic SDH variants

46. Clinical experience with the AKT1 inhibitor miransertib in two children with PIK3CA-related overgrowth syndrome

47. C2.2 Postzygotic activating variants in mapk pathway genes cause intracranial and extracranial vascular malformations that respond to targeted inhibition

48. SDHA related tumorigenesis: a new case series and literature review for variant interpretation and pathogenicity

49. Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB , SDHC and SDHD .

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