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52. Jet Launching Radius in Low-Power Radio-Loud AGNs in Advection-Dominated Accretion Flows

56. Extended gene panel testing in lobular breast cancer

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.

68. Academic accomplishments of Black neurosurgeons in the United States

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

73. Elusive Phenomena, Unwieldy Things

81. The Geologic Time Spiral-A Path to the Past. General Interest Publication 58.

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

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

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

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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