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Results 1-10 of 21 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2002
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
Cundy, T.
;
Hegde, M.
;
Naot, D.
;
Chong, B.
;
King, A.
;
Wallace, R.
;
Mulley, J.
;
Love, D.
;
Seidel, J.
;
Fawkner, M.
;
Banovic, T.
;
Callon, K.
;
Grey, A.
;
Reid, I.
;
Middleton-Hardie, C.
;
Cornish, J.
2002
Sodium-channel defects in benign familial neonatal-infantile seizures
Heron, S.
;
Crossland, K.
;
Andermann, E.
;
Phillips, H.
;
Hall, A.
;
Bleasel, A.
;
Shevell, M.
;
Mercho, S.
;
Seni, M.
;
Guiot, M.
;
Mulley, J.
;
Berkovic, S.
;
Scheffer, I.
2005
A community-based intervention to reduce antibiotic use for upper respiratory tract infections in regional South Australia
Dollman, W.
;
LeBlanc, V.
;
Stevens, L.
;
O'Connor, P.
;
Turnidge, J.
2007
Low CD4 T cell immunity to pneumolysin is associated with nasopharyngeal carriage of pneumococci in children
Zhang, Q.
;
Bagrade, L.
;
Bernatoniene, J.
;
Clarke, E.
;
Paton, J.
;
Mitchell, T.
;
Nunez, D.
;
Finn, A.
2013
Rare variants in single-minded 1 (SIM1) are associated with severe obesity
Ramachandrappa, S.
;
Raimondo, A.
;
Cali, A.
;
Keogh, J.
;
Henning, E.
;
Saeed, S.
;
Thompson, A.
;
Garg, S.
;
Bochukova, E.
;
Brage, S.
;
Trowse, V.
;
Wheeler, E.
;
Sullivan, A.
;
Dattani, M.
;
Clayton, P.
;
Datta, V.
;
Bruning, J.
;
Wareham, N.
;
O'Rahilly, S.
;
Peet, D.
;
et al.
2004
Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathy
Berkovic, S.
;
Heron, S.
;
Giordano, L.
;
Marini, C.
;
Guerrini, R.
;
Kaplan, R.
;
Gambardella, A.
;
Steinlein, O.
;
Grinton, B.
;
Dean, J.
;
Bordo, L.
;
Hodgson, B.
;
Yamamoto, T.
;
Mulley, J.
;
Zara, F.
;
Scheffer, I.
2003
X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3
Gedeon, A.
;
Nelson, J.
;
Gecz, J.
;
Mulley, J.
2011
MLVA and phage typing as complementary tools in the epidemiological investigation of Salmonella enterica serovar typhimurium clusters
Ross, I.
;
Davos, D.
;
Mwanri, L.
;
Raupach, J.
;
Heuzenroeder, M.
2003
Analysis of CFTR mutation screening in cases of isolated fetal echogenic bowel in the South Australian population
Nicholls, C.
;
Nelson, P.
;
Poplawski, N.
;
Chin, S.
;
Fong, B.
;
Solly, P.
;
Fietz, M.
;
Fletcher, J.
2003
Dietry intakes and food sources of omega-6 and omega-3 polyunsaturated fatty acids
Meyer, B.
;
Mann, N.
;
Lewis, J.
;
Milligan, G.
;
Sinclair, A.
;
Howe, P.
Discover
Author
7
Mulley, J.
5
Berkovic, S.
5
Scheffer, I.
4
Wallace, R.
3
Dibbens, L.
3
Grinton, B.
3
Heron, S.
3
Hodgson, B.
2
Andermann, E.
2
Davos, D.
.
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Subject
21
Female
15
Adult
14
Adolescent
13
Infant
12
Middle Aged
10
Pedigree
7
Aged
6
Mutation, Missense
4
Australia
4
DNA Mutational Analysis
.
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Date issued
4
2010 - 2013
17
2002 - 2009