StephenBDowtonMD

PubMed

• 1 citations
  The benefits of international health experiences for Australian and New Zealand medical education
  H. Patrick McNeil, Paul Wild, Hayley Harris, S. Bruce Dowton> ;The Medical Journal of Australia. 2017 Jun 1
• An opportunity to reinforce ethical values: declarations made by graduating medical students in Australia and New Zealand.
  Macneill, P. U., May, A. N., Dowton, S. B.> ;Intern Med J. 2009 Feb
• An innovative outcomes-based medical education program built on adult learning principles.
  McNeil, H. P., Hughes, C. S., Toohey, S. M., Dowton, S. B.> ;Med Teach. 2006 Sep
• Plasma proteins in health and disease: a scientific symposium to celebrate the career and accomplishments of Harvey R. Colten, M.D.
  Fontan, J. P., Dowton, S. B., Perlmutter, D., Gitlin, J., Cole, F. S.> ;Pediatr Res. 2006 Aug
• Imperatives in medical education and training in response to demands for a sustainable workforce.
  Dowton, S. B.> ;Med J Aust. 2005 Dec 13
• 26 citations
  Postgraduate medical education: rethinking and integrating a complex landscape.
  S. Bruce Dowton, Marie Louise Stokes, Evan J. Rawstron, Philip R. Pogson, Mark Brown> ;The Medical Journal of Australia. 2005 Feb 21
• 20 citations
  Leadership in medicine: where are the leaders?
  S. Bruce Dowton> ;The Medical Journal of Australia. 2004 Dec 6
• Training our future rural medical workforce.
  Dowton, S. B., Brown, D.> ;Med J Aust. 2004 Jun 21
• Declarations made by graduating medical students in Australia and New Zealand.
  McNeill, P. M., Dowton, S. B.> ;Med J Aust. 2002 Feb 4
• Reinventing ourselves.
  Coiera, E., Dowton, S. B.> ;Med J Aust. 2000 Oct 2
• Vertebral anomalies in a new family with ODED syndrome.
  Piersall, L. D., Dowton, S. B., McAlister, W. H., Waggoner, D. J.> ;Clin Genet. 2000 Jun
• Partial monosomy of distal 10q: three new cases and a review.
  Waggoner, D. J., Chow, C. K., Dowton, S. B., Watson, M. S.> ;Am J Med Genet. 1999 Sep 3
• Deletion of 1q in a patient with acrofacial dysostosis.
  Waggoner, D. J., Ciske, D. J., Dowton, S. B., Watson, M. S.> ;Am J Med Genet. 1999 Feb 12
• Methylmalonic aciduria (cblF): case report and response to therapy.
  Waggoner, D. J., Ueda, K., Mantia, C., Dowton, S. B.> ;Am J Med Genet. 1998 Oct 12
• Unique cardiac and cerebral anomalies with chondrodysplasia punctata.
  Ciske, D. J., Waggoner, D. J., Dowton, S. B.> ;Am J Med Genet. 1998 Jan 6
• Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects.
  Dowton, S. B., Hing, A. V., Sheen-Kaniecki, V., Watson, M. S.> ;J Med Genet. 1997 May
• Respiratory complications of Ehlers-Danlos syndrome type IV.
  Dowton, S. B., Pincott, S., Demmer, L.> ;Clin Genet. 1996 Dec
• Need for velopharyngeal management following palatoplasty: an outcome analysis of syndromic and nonsyndromic patients with Robin sequence.
  Witt, P. D., Myckatyn, T., Marsh, J. L., Grames, L. M., Dowton, S. B.> ;Plast Reconstr Surg. 1997 May
• Serum amyloid A gene expression in rabbit, mink and mouse.
  Marhaug, G., Hackett, B., Dowton, S. B.> ;Clin Exp Immunol. 1997 Feb
• Grouped papules in Hurler-Scheie syndrome.
  Schiro, J. A., Mallory, S. B., Demmer, L., Dowton, S. B., Luke, M. C.> ;J Am Acad Dermatol. 1996 Nov
• A novel missense mutation in the exon containing the putative ornithine-binding domain of the OTC enzyme in a female.
  Demmer, L. A., Kim, J. M., de Martinville, B., Dowton, S. B.> ;Hum Mutat. 1996
• Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2.
  Ho, C. Y., Otterud, B., Legare, R. D., Varvil, T., Saxena, R., DeHart, D. B., Kohler, S. E., Aster, J. C., Dowton, S. B., Li, F. P., Leppert, M., Gilliland, D. G.> ;Blood. 1996 Jun 15
• Nonketotic hyperglycinemia: atypical clinical and biochemical manifestations.
  Steiner, R. D., Sweetser, D. A., Rohrbaugh, J. R., Dowton, S. B., Toone, J. R., Applegarth, D. A.> ;J Pediatr. 1996 Feb
• Linkage of preaxial polydactyly type 2 to 7q36.
  Hing, A. V., Helms, C., Slaugh, R., Burgess, A., Wang, J. C., Herman, T., Dowton, S. B., Donis-Keller, H.> ;Am J Med Genet. 1995 Aug 28
• Schinzel-Giedion syndrome and congenital megacalyces.
  Herman, T. E., Sweetser, D. A., McAlister, W. H., Dowton, S. B.> ;Pediatr Radiol. 1993
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