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Results 1-10 of 40 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1998Sexual dimorphism of the somatotrophic axisGatford, K.; Egan, A.; Clarke, I.; Owens, P.
1998Coexistence of Gaucher-Disease Type 1 and Joubert-SyndromeVan Royen-Kerkhof, A.; Pollthe, B.; Kleijer, W.; van Diggelen, O.; Aerts, J.; Hopwood, J.; Beemer, F.
1998Effect of Parity, Gravidity, Previous Miscarriage, and Age On Risk of Downs-Syndrome - Population Based StudyChan, A.; McCaul, K.; Keane, R.; Haan, E.
1998A population-based study of abdominal wall defects in South Australia and Western AustraliaByron-Scott, R.; Haan, E.; Chan, A.; Bower, C.; Scott, H.; Clark, K.
1998Transcranial correction of orbital neurofibromatosisSnyder, B.; Hanieh, A.; Trott, J.; David, D.
1998Asthma and other atopic diseases in Australian children. Australian arm of the International Study of Asthma and Allergy in ChildhoodRobertson, C.; Dalton, M.; Peat, J.; Haby, M.; Bauman, A.; Kennedy, J.; Landau, L.
1998Haemolytic-uraemic syndrome outbreak caused by Escherichia coli O111:H-: clinical outcomesHenning, P.; Tham, E.; Martin, A.; Beare, T.; Jureidini, K.
1998X-linked adrenoleukodystrophy: the Australasian experienceKirk, E.; Fletcher, J.; Sharp, P.; Carey, B.; Poulos, A.
1998Identification of a common mutation (R245h) in Sanfilippo A patients from the NetherlandsWeber, B.; Vandekamp, J.; Kleijer, W.; Guo, X.H.; Blanch, L.; van Diggelen, O.; Wevers, R.; Poorthuis, B.; Hopwood, J.
1998Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: nine novel mutations including T312S, a common allele that confers a mild phenotypeYamada, N.; Fukuda, S.; Tomatsu, S.; Muller, V.; Hopwood, J.; Nelson, J.; Kato, Z.; Yamagishi, A.; Sukegawa, K.; Kondo, M.; Orii, T.