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Journal of Medical Genetics|February 1, 1985
Trigonocephaly and the Opitz C syndromeC Sargent, J Burn, M Baraitser, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
Progression of gait dysfunction in incident Parkinson's disease: impact of medication and phenotypeBrook Galna, Sue Lord, David J Burn, et al.Journal of Medical Genetics|August 1, 1986
Autosomal dominant thoracolaryngopelvic dysplasia: Barnes syndromeJ Burn, C Hall, D Marsden, et al.Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|June 26, 2001
Adenocarcinoma of the rat esophagus in the presence of a proton pump inhibitor: a pilot studyK H Moore, P Barry, J Burn, et al.Clinical Dysmorphology|October 1, 1994
Autosomal dominant transmission of Pallister-Hall syndromeM Penman Splitt, C Wright, R Perry, et al.Journal of Medical Genetics|October 1, 1993
DiGeorge syndrome: part of CATCH 22D I Wilson, J Burn, P Scambler, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1994
Differential diagnosis of Parkinson's disease, multiple system atrophy, and Steele-Richardson-Olszewski syndrome: discriminant analysis of striatal 18F-dopa PET dataD J Burn, G V Sawle, D J BrooksJournal of Medical Genetics|June 1, 1984
Orofaciodigital syndrome with mesomelic limb shorteningJ Burn, C Dezateux, C M Hall, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2006
Clinical phenotype of subjects with Parkinson's disease and orthostatic hypotension: autonomic symptom and demographic comparisonLiesl M Allcock, Rose Anne Kenny, David J BurnClinical Genetics|December 1, 1996
Further evidence of genetic heterogeneity in hereditary hydronephrosisD McHale, M E Porteous, J Wentzel, et al.Pageof 51