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51. Additional file 2 of Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applications

54. TP53 Mutation Status Defines a Distinct Clinicopathological Entity of Therapy-Related Myeloid Neoplasm, Characterized By Genomic Instability and Extremely Poor Outcome

55. Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in RUNX1, GATA2 and DDX41

56. Allogeneic Hematopoietic Stem Cell Transplant Outcomes in Adults with Inherited Myeloid Malignancies

57. Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation

58. Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis

61. Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

62. ARMC5 is part of an RPB1-specific ubiquitin ligase implicated in adrenal hyperplasia

63. Molecular therapy selection in treatment-refractory advanced cancers: A retrospective cohort study determining the utility of TOPOGRAPH knowledge base.

64. Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations

67. GATA2 is required for lymphatic vessel valve development and maintenance

68. Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature

69. The clinical and genetic features of hereditary pancreatitis in South Australia

70. Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema

72. Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome

73. Childhood acute myeloid leukemia shows a high level of germline predisposition

76. Cover, Volume 42, Issue 11

81. Brief Report: Identification of a Pathogenic Variant in TREX1 in Early-Onset Cerebral Systemic Lupus Erythematosus by Whole-Exome Sequencing

82. GATA2 deficiency syndrome: A decade of discovery

83. The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

84. Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability

85. Additional file 3 of Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia

86. Additional file 2 of Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia

87. Additional file 4 of Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia

88. Additional file 1 of Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia

89. Childhood acute myeloid leukemia shows a high level of germline predisposition

90. Comparison of World Health Organization and International Consensus Classification Guidelines for Myeloid Neoplasms Harboring TP53-Mutations Using an Independent International Cohort

92. Single-Hit TP53mut Is Associated with Poor Outcomes in Therapy-Related but Not De Novo Myelodysplastic Syndromes: Importance of Clinical History

93. Interferon autoantibodies associated with AIRE deficiency decrease the expression of IFN-stimulated genes

97. ARMC5 Mutations Are Common in Familial Bilateral Macronodular Adrenal Hyperplasia

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