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Journal of Medical Genetics|October 1, 1986
A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndromeR D Jefferson, J Burn, K L Gaunt, et al.The British Journal of Radiology|May 19, 2000
Distribution of cranial MRI abnormalities in patients with symptomatic and subclinical CADASILA Coulthard, S C Blank, K Bushby, et al.Oncogene|March 21, 1996
The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumour suppressor gene involved in the development of cylindromasP J Biggs, P Chapman, S R Lakhani, et al.Neuropsychologia|October 19, 2013
The basal ganglia in perceptual timing: timing performance in Multiple System Atrophy and Huntington's diseaseThomas E Cope, Manon Grube, Baldev Singh, et al.Acta Endocrinologica|November 1, 1982
Impaired subcutaneous absorption of insulin in 'brittle' diabeticsP D Home, M Massi-Benedetti, G V Gill, et al.Diabetologia|April 11, 2003
Nitric oxide synthase gene polymorphisms and diabetic nephropathyJ D Rippin, A Patel, N D Belyaev, et al.Journal of Medical Genetics|May 1, 1988
Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosisC P Bennett, J Burn, G E Moore, et al.The British Journal of Surgery|October 1, 1995
Clinical impact of colonoscopic screening in first-degree relatives of patients with hereditary non-polyposis colorectal cancerS E Green, P D Chapman, J Burn, et al.Parkinson'S Disease|June 1, 2018
Coping with Cognitive Impairment in People with Parkinson's Disease and Their Carers: A Qualitative StudyRachael A Lawson, Daniel Collerton, John-Paul Taylor, et al.Gut|November 4, 2008
Cell kinetics and gene expression changes in colorectal cancer patients given resistant starch: a randomised controlled trialS S Dronamraju, J M Coxhead, S B Kelly, et al.Pageof 57