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1. A Generation of Crisis-Responsive Reintegration in Migration Management: Reflections from the Philippines

5. Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

6. Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

7. Experience of Use of an Artificial Neural Network as an Auxiliary in the Physical Fitness Classification of Taekwondo Athletes from Mexico City

12. Mendelian randomisation study of smoking exposure in relation to breast cancer risk

13. Mendelian randomisation study of smoking exposure in relation to breast cancer risk.

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

15. Speech and language deficits are central to SETBP1 haploinsufficiency disorder

16. Speech and language deficits are central to SETBP1 haploinsufficiency disorder

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

19. EP03.02: Long‐term developmental outcomes of children with a prenatal diagnosis of a variant of uncertain significance: the PrenatAL Microarray (PALM) study.

23. Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice

24. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

25. Publisher Correction: Homologous recombination DNA repair defects in PALB2-associated breast cancers (npj Breast Cancer, (2019), 5, 1, (23), 10.1038/s41523-019-0115-9)

26. Development and validation of a targeted gene sequencing panel for application to disparate cancers

27. Homologous recombination DNA repair defects in PALB2-associated breast cancers

28. Homologous recombination DNA repair defects in PALB2-associated breast cancers

29. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

30. Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants

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

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

35. A national approach to rapid genomic diagnosis in acute pediatrics.

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

37. A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system.

38. Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening.

39. Baby beyond hearing, Using genomics as a newborn screening tool.

40. Homologous recombination DNA repair defects in PALB2-associated breast cancers.

41. What to do with a negative exome?.

42. The first 500 diagnostic exomes: A demonstration of safety, clinical utility, translation and cost-effectiveness.

43. Whole exome sequencing in infants with congenital hearing loss.

44. Publisher Correction: Homologous recombination DNA repair defects in PALB2-associated breast cancers (npj Breast Cancer, (2019), 5, 1, (23), 10.1038/s41523-019-0115-9).

45. Childhood hearing Australasian Medical Professionals (CHAMP) network: Consensus guidelines recommendations on etiological investigation and clinical medical management of childhood hearing loss in Australia.

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

47. The incidence, prevalence and clinical features of MECP2 duplication syndrome in Australian children

48. Homologous recombination DNA repair defects in PALB2-associated breast cancers (vol 5, 23, 2019)

49. Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations

50. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

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