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Results 31-40 of 41 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2005
Early onset seizures and Rett-like features associated with mutations in CDKL5
Evans, J.
;
Archer, H.
;
Colley, J.
;
Ravn, K.
;
Nielsen, J.
;
Kerr, A.
;
Williams, E.
;
Christodoulou, J.
;
Gecz, J.
;
Jardine, P.
;
Wright, M.
;
Pilz, D.
;
Lazarou, L.
;
Cooper, D.
;
Sampson, J.
;
Butler, R.
;
Whatley, S.
;
Clarke, A.
2005
Enzyme replacement therapy for Gaucher disease in Australia
Goldblatt, J.
;
Szer, J.
;
Fletcher, J.
;
McGill, J.
;
Rowell, J.
;
Wilson, M.
2006
Case for varicella surveillance in Australia
Peadon, E.
;
Burgner, D.
;
Nissen, M.
;
Buttery, J.
;
Zurynski, Y.
;
Elliott, E.
;
Gold, M.
;
Marshall, H.
;
Booy, R.
2004
Asthma in emergency departments: combined adult and paediatric versus paediatric only centres
Powell, C.
;
Raftos, J.
;
Kerr, D.
;
Rosengarten, P.
;
Kelly, A.
2001
Nationwide study of haemolytic uraemic syndrome: clinical, microbiological, and epidemiological features
Elliott, E.
;
Robins-Browne, R.
;
O'Loughlin, E.
;
Bennett-Wood, V.
;
Bourke, J.
;
Henning, P.
;
Hogg, G.
;
Knight, J.
;
Powell, H.
;
Redmond, D.
2009
Collagen type III alpha 1 is a gastro-oesophageal reflux disease susceptibility gene and a male risk factor for hiatus hernia
Asling, B.
;
Jirholt, J.
;
Hammond, P.
;
Knutsson, M.
;
Walentinsson, A.
;
Davidson, G.
;
Agreus, L.
;
Lehmann, A.
;
Lagerstrom-Fermer, M.
2009
A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology
Talseth-Palmer, B.
;
Bowden, N.
;
Meldrum, C.
;
Nicholl, J.
;
Thompson, E.
;
Friend, K.
;
Liebelt, J.
;
Bratkovic, D.
;
Haan, E.
;
Yu, S.
;
Scott, R.
2009
A Novel Bocavirus Associated with Acute Gastroenteritis in Australian Children
Arthur, J.
;
Higgins, G.
;
Davidson, G.
;
Givney, R.
;
Ratcliff, R.
;
Münger, K.
2002
Generalized epilepsy with febrile seizures plus: Mutation of the sodium channel subunit SCN1B
Wallace, R.
;
Scheffer, I.
;
Parasivam, G.
;
Barnett, S.
;
Wallace, G.
;
Sutherland, G.
;
Berkovic, S.
;
Mulley, J.
2006
Detection of mucopolysaccharidosis type II by measurement of iduronate-2-sulfatase in dried blood spots and plasma samples
Dean, C.
;
Bockmann, M.
;
Hopwood, J.
;
Brooks, D.
;
Meikle, P.
Discover
Author
5
Fletcher, J.
4
Davidson, G.
4
Gold, M.
4
Hopwood, J.
4
Meikle, P.
3
Butler, R.
3
Gecz, J.
3
Goldwater, P.
3
Haan, E.
2
Bettelheim, K.
.
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Subject
41
Humans
34
Child, Preschool
27
Adolescent
23
Female
23
Male
14
Adult
14
Infant, Newborn
10
Australia
7
Mutation
6
Middle Aged
.
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Date issued
6
2009
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2008
4
2007
3
2006
7
2005
3
2004
1
2003
7
2002
2
2001
7
2000
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