about
Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defectsVertebral anomalies in a new family with ODED syndrome.Respiratory complications of Ehlers-Danlos syndrome type IV.Interhemispheric transfer in children with early-treated phenylketonuria.An opportunity to reinforce ethical values: declarations made by graduating medical students in Australia and New Zealand.Declarations made by graduating medical students in Australia and New Zealand.The benefits of international health experiences for Australian and New Zealand medical education.An innovative outcomes-based medical education program built on adult learning principles.Serum amyloid A gene expression in rabbit, mink and mouse.Lesions in oculocerebrorenal syndromeSerum amyloid-P component of the Armenian hamster: gene structure and comparison with structure and expression of the SAP gene from Syrian hamsterPredictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2AReinventing ourselvesNeed for velopharyngeal management following palatoplasty: an outcome analysis of syndromic and nonsyndromic patients with Robin sequenceDeletion of 1q in a patient with acrofacial dysostosisMethylmalonic aciduria (cblF): case report and response to therapyTraining our future rural medical workforceLeadership in medicine: where are the leaders?Bending the quality curveAssessing the quality of care for paediatric depression and anxiety in Australia: A population-based sample survey
P50
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P50
description
researcher
@en
name
Dowton SB
@nl
Stephen B. Dowton
@en
type
label
Dowton SB
@nl
Stephen B. Dowton
@en
altLabel
Dowton SB
@en
prefLabel
Dowton SB
@nl
Stephen B. Dowton
@en
P106
P31
P496
0000-0003-0828-1073