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Clinical Endocrinology|April 1, 1985
A case of 'essential' hypernatraemia due to resetting of the osmostatG Gill, P Baylis, J BurnJournal of Medical Genetics|January 1, 1991
Oculofacialbulbar palsy in mother and son: review of 26 reports of familial transmission within the 'Möbius spectrum of defects'K D MacDermot, R M Winter, D Taylor, et al.Acta Neurologica Scandinavica|November 11, 2009
Natural history, symptoms and treatment of the narcoleptic syndromeJ D Parkes, M Baraitser, C D Marsden, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1982
Joubert-Boltshauser syndrome with polydactyly in siblingsJ Egger, M H Bellman, E M Ross, et al.American Journal of Medical Genetics|January 30, 1995
Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndromeW Reardon, R J Gibbons, R M Winter, et al.Journal of Medical Genetics|February 1, 1991
Pitfalls in counselling: the craniosynostosesR Marini, K Temple, L Chitty, et al.The Lancet. Neurology|July 10, 2003
Progressive supranuclear palsy: where are we now?David J Burn, Andrew J LeesMovement Disorders : Official Journal of the Movement Disorder Society|September 23, 2003
Current treatment of dementia with Lewy bodies and dementia associated with Parkinson's diseaseDavid J Burn, Ian G McKeithClinical Dysmorphology|January 29, 2000
Severe microcephaly, choreiform movements, cataracts and sensorineural deafness in two patients: a new syndrome?A S Plomp, M Baraitser, S F Slaney, et al.Pageof 60