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Issue Date
Title
Author(s)
2015
Five-year survival of children with chronic critical illness in Australia and New Zealand
Namachivayam, S.
;
Alexander, J.
;
Slater, A.
;
Millar, J.
;
Erickson, S.
;
Tibballs, J.
;
Festa, M.
;
Ganu, S.
;
Segedin, L.
;
Schlapbach, L.
;
Williams, G.
;
Shann, F.
;
Butt, W.
2015
A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype
Terhal, P.
;
Nievelstein, R.
;
Verver, E.
;
Topsakal, V.
;
van Dommelen, P.
;
Hoornaert, K.
;
Le Merrer, M.
;
Zankl, A.
;
Simon, M.
;
Smithson, S.
;
Marcelis, C.
;
Kerr, B.
;
Clayton-Smith, J.
;
Kinning, E.
;
Mansour, S.
;
Elmslie, F.
;
Goodwin, L.
;
van der Hout, A.
;
Veenstra-Knol, H.
;
Herkert, J.
;
et al.
2018
The multifaceted presentation of chronic recurrent multifocal osteomyelitis: a series of 486 cases from the Eurofever international registry
Girschick, H.
;
Finetti, M.
;
Orlando, F.
;
Schalm, S.
;
Insalaco, A.
;
Ganser, G.
;
Nielsen, S.
;
Herlin, T.
;
Koné-Paut, I.
;
Martino, S.
;
Cattalini, M.
;
Anton, J.
;
Al-Mayouf, S.
;
Hofer, M.
;
Quartier, P.
;
Boros, C.
;
Kuemmerle-Deschner, J.
;
Pires Marafon, D.
;
Alessio, M.
;
Schwarz, T.
;
et al.
2014
Outcomes of repair of complete atrioventricular septal defect in the current era
Xie, O.
;
Brizard, C.
;
D'udekem, Y.
;
Galati, J.
;
Kelly, A.
;
Yong, M.
;
Weintraub, R.
;
Konstantinov, I.
2014
Development of paediatric biochemistry centile charts as a complement to laboratory reference intervals
Loh, T.
;
Antoniou, G.
;
Baghurst, P.
;
Metz, M.
2014
Oxygen saturation targeting in preterm infants receiving continuous positive airway pressure
Lim, K.
;
Wheeler, K.
;
Gale, T.
;
Jackson, H.
;
Kihlstrand, J.
;
Sand, C.
;
Dawson, J.
;
Dargaville, P.
2013
PRRT2 mutation in Japanese children with benign infantile epilepsy
Okumura, A.
;
Shimojima, K.
;
Kubota, T.
;
Abe, S.
;
Yamashita, S.
;
Imai, K.
;
Okanishi, T.
;
Enoki, H.
;
Fukasawa, T.
;
Tanabe, T.
;
Dibbens, L.
;
Shimizu, T.
;
Yamamoto, T.
2014
Genetics of hereditary neurological disorders in children
Huang, Y.
;
Yu, S.
;
Wu, Z.
;
Tang, B.
2011
An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutations
Ratnayake, P.
;
Wakefield, C.
;
Meiser, B.
;
Suthers, G.
;
Price, M.
;
Duffy, J.
;
Tucker, K.
2010
The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletion
MacKinnon, R.
;
Selan, C.
;
Wall, M.
;
Baker, E.
;
Nandurkar, H.
;
Campbell, L.
Discover
Author
84
et al.
64
Grzeskowiak, L.
62
Makrides, M.
61
Gecz, J.
60
Marshall, H.
58
Mol, B.
45
Sawyer, M.
41
Gold, M.
39
Clifton, V.
32
Omari, T.
.
next >
Subject
11
92 Health
10
11 Medical and Health Sciences
7
9201 Clinical Health (Organs, Dis...
6
1114 Paediatrics and Reproductive...
5
06 Biological Sciences
5
0604 Genetics
4
060403 Developmental Genetics (in...
4
1103 Clinical Sciences
4
110311 Medical Genetics (excl. Ca...
4
111403 Paediatrics
.
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Date issued
27
2019
63
2018
69
2017
61
2016
143
2015
155
2014
186
2013
184
2012
126
2011
173
2010
.
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