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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.Journal of Medical Genetics|October 1, 1990
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult maleF Martin, J Platt, E J Tawn, et al.Clinical Dysmorphology|April 1, 1993
Agnathia-holoprosencephaly: a new recessive syndrome?M E Porteous, C Wright, D Smith, et al.Postgraduate Medical Journal|January 5, 2000
Extrinsic cerebral venous sinus obstruction resulting in intracranial hypertensionP Goldsmith, D J Burn, A Coulthard, et al.BMJ (Clinical Research Ed.)|February 11, 1989
Congenital hypertrophy of retinal pigment epithelium: a sign of familial adenomatous polyposisP D Chapman, W Church, J Burn, et al.Australian Veterinary Journal|April 21, 2010
Isolation of bovine herpesvirus type 5 from the semen of a healthy bull in AustraliaI S Diallo, G R Hewitson, J Hoad, et al.Pageof 49