3,945 results on '"Newman, William"'
Search Results
52. Jet Launching Radius in Low-Power Radio-Loud AGNs in Advection-Dominated Accretion Flows
53. Drip and Ship versus Mothership Model in the Middle Cerebral Artery Stroke: A Propensity-Matched Real-World Analysis Through National Inpatient Sample Data
54. Isaac Newton’s Atomist Sources: The Case of Bernhard Varenius
55. Evaluation of the Manchester COVID-19 Urgent Eyecare Service (CUES)
56. Extended gene panel testing in lobular breast cancer
57. New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder
58. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
59. Breast cancer risks associated with missense variants in breast cancer susceptibility genes
60. Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci
61. Recommendations for clinical interpretation of variants found in non-coding regions of the genome
62. Common variants in breast cancer risk loci predispose to distinct tumor subtypes
63. Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study
64. Exploring NICU nurses' views of a novel genetic point‐of‐care test identifying neonates at risk of antibiotic‐induced ototoxicity: A qualitative study.
65. Salvage resection of recurrent previously irradiated brain metastases: tumor control and radiation necrosis dependency on adjuvant re-irradiation
66. A remarkable infestation of epibionts and endobionts of an edible chiton (Polyplacophora: Chitonidae) from the Mexican tropical Pacific
67. Public preferences for pharmacogenetic testing in the NHS: Embedding a discrete choice experiment within service design to better meet user needs
68. Academic accomplishments of Black neurosurgeons in the United States
69. Separation Surgery for Metastatic Spine Tumors: How Less Became More
70. Genetic testing in the acute setting : a round table discussion
71. Clinical utility of testing for PALB2 and CHEK2 c.1100delC in breast and ovarian cancer
72. Mendelian randomisation study of smoking exposure in relation to breast cancer risk
73. Elusive Phenomena, Unwieldy Things
74. Earthquake Complexity
75. Daniel Sennert’s Response to Santorio Santori in the Light of Chymical Atomism
76. Direct laser frequency comb calibration of an astronomical spectrograph
77. Newton the Alchemist
78. Reassurance on false negatives in the Manchester COVID19 Urgent Eyecare Service (CUES)
79. Rampling and the Ripley Corpus: Jennifer M. Rampling: The experimental fire: inventing English alchemy, 1300–1700. Chicago: University of Chicago Press, 2020, 416pp, $35.00 HB
80. The effect of surgery on radiation necrosis in irradiated brain metastases: extent of resection and long-term clinical and radiographic outcomes
81. The Geologic Time Spiral-A Path to the Past. General Interest Publication 58.
82. Development and implementation of a Greater Manchester COVID19 Urgent Eyecare Service
83. Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome.
84. Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformations
85. Neurologic, Oncologic, Mechanical, and Systemic and Other Decision Frameworks for Spinal Disease
86. Living with Dysphagia: A Survey Exploring the Experiences of Adults Living with Neuromuscular Disease and their Caregivers in the United Kingdom
87. Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome
88. Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data
89. Population screening requires robust evidence—genomics is no exception
90. Deep intronic variant causes aberrant splicing of ATP7A in a family with a variable occipital horn syndrome phenotype
91. Population based germline testing of BRCA1, BRCA2 and PALB2 in breast cancer patients in the UK: Evidence to support extended testing and definition of groups who may not require testing
92. The rise of point-of-care genetics: how the SARS-CoV-2 pandemic will accelerate adoption of genetic testing in the acute setting
93. Enzyme replacement therapy and hematopoietic stem cell transplant: a new paradigm of treatment in Wolman disease
94. Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidine
95. Loss-of-function variants in myocardin cause congenital megabladder in humans and mice
96. Classification and correlation of RYR2 missense variants in individuals with catecholaminergic polymorphic ventricular tachycardia reveals phenotypic relationships
97. Clinical utility of genetic testing in 201 preschool children with inherited eye disorders
98. A recurrent missense variant in HARS2 results in variable sensorineural hearing loss in three unrelated families
99. Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome.
100. Prolonged spontaneous emission and dephasing of localized excitons in air-bridged carbon nanotubes
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