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3. Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum

5. The impact of coding germline variants on contralateral breast cancer risk and survival

6. Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711

7. Fitting manifestations : epiphany in Alice Oswald, Kathleen Jamie, Liz Berry and Joanne Dixon

8. Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

9. Delineation of the 3p14.1p13 Microdeletion Associated With Syndromic Distal Limb Contractures

11. CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

13. Genome-wide association study identifies novel breast cancer susceptibility loci

16. Update of PAX2 Mutations in Renal Coloboma Syndrome and Establishment of a Locus-Specific Database†

17. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

20. Constraint and conservation of paired‐type homeodomains predicts the clinical outcome of missense variants of uncertain significance

21. Starting out right: early education and looked after children

22. Purl

23. ‘Brightness and Unfixity: reframing epiphany in Alice Oswald’s Woods etc.’

24. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

29. Step Change : an evaluation

30. STAC3variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility

32. A pilot study of exome sequencing in a diverse New Zealand cohort with undiagnosed disorders and cancer

34. Annexin A1 expression in a pooled breast cancer series: Association with tumor subtypes and prognosis

35. STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility.

36. Mutations in CDC45 , Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis

37. Annexin A1 expression in a pooled breast cancer series: Association with tumor subtypes and prognosis

38. Attitudes of nonpalliative care nurses towards palliative care

42. Mutations in NOTCH1 Cause Adams-Oliver Syndrome

43. Genotype and clinical care correlations in craniosynostosis : Findings from a cohort of 630 Australian and New Zealand patients

44. FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair

48. De novo mutations in the mitochondrialND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency

49. Correction: Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711

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