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Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|March 19, 2013
Dosimetric and clinical impact of 3D vs. 2D planning in palliative radiotherapy for bone metastasesKathy Pope, David Fitzpatrick, Andrew Potter, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 18, 2016
Early adjuvant radiotherapy in the treatment of atypical meningiomaMichael D Jenkinson, Mueez Waqar, Jibril Osman Farah, et al.European Journal of Medical Genetics|January 13, 2023
Expanding the neurodevelopmental phenotype associated with HK1 de novo heterozygous missense variantsRebecca L Poole, Mihaly Badonyi, Alison Cozens, et al.American Journal of Medical Genetics. Part A|September 14, 2007
WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformationsMohnish Suri, Peter Kelehan, David O'neill, et al.International Journal of Radiation Oncology, Biology, Physics|May 18, 2012
A one-step cone-beam CT-enabled planning-to-treatment model for palliative radiotherapy-from development to implementationRebecca K S Wong, Daniel Letourneau, Anita Varma, et al.Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine|March 22, 2019
Epidemiology of emergency ambulance service calls related to mental health problems and self harm: a national record linkage studyEdward A S Duncan, Catherine Best, Nadine Dougall, et al.European Journal of Human Genetics : EJHG|October 16, 2008
Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearanceJill Clayton-Smith, Sarah Walters, Emma Hobson, et al.Human Genetics|January 11, 2007
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardationVera M Kalscheuer, David FitzPatrick, Niels Tommerup, et al.Nature Neuroscience|March 3, 2017
Video-rate volumetric functional imaging of the brain at synaptic resolutionRongwen Lu, Wenzhi Sun, Yajie Liang, et al.Nature Genetics|October 12, 2004
Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1BSandra Hanks, Kim Coleman, Sarah Reid, et al.Pageof 15