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Issue Date
Title
Author(s)
2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
Dibbens, L.
;
Tarpey, P.
;
Hynes, K.
;
Bayly, M.
;
Scheffer, I.
;
Smith, R.
;
Bomar, J.
;
Sutton, E.
;
Vandeleur, L.
;
Shoubridge, C.
;
Edkins, S.
;
Turner, S.
;
Stevens, C.
;
O'Meara, S.
;
Tofts, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Halliday, K.
;
Jones, D.
;
et al.
1995
An integrated physical map of human chromosome 16
Doggett, N.
;
Goodwin, L.
;
Tesmer, J.
;
Meincke, L.
;
Bruce, D.
;
Clark, L.
;
Altherr, M.
;
Ford, A.
;
Chi, H.C.
;
Marrone, B.
;
Longmire, J.
;
Lane, S.
;
Whitmore, S.
;
Lowenstein, N.
;
Sutherland, G.
;
Mundt, M.
;
Knill, E.
;
Bruno, W.
;
Macken, C.
;
Torney, D.
;
et al.
2007
Epidemiological comparisons of problems and positive qualities reported by adolescents in 24 countries
Rescorla, L.
;
Achenbach, T.
;
Ivanova, M.
;
Dumenci, L.
;
Almqvist, F.
;
Bilenberg, N.
;
Bird, H.
;
Broberg, A.
;
Dobrean, A.
;
Dopfner, M.
;
Erol, N.
;
Forns, M.
;
Hannesdottir, H.
;
Kanbayashi, Y.
;
Lambert, M.
;
Leung, P.
;
Minaei, A.
;
Mulatu, M.
;
Novik, T.
;
Oh, K.
;
et al.
1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
Muenke, M.
;
Gripp, K.
;
McDonald-McGinn, D.
;
Gaudenz, K.
;
Whitaker, L.
;
Bartlett, S.
;
Markowitz, R.
;
Robin, N.
;
Nwokoro, N.
;
Mulvihill, J.
;
Losken, H.
;
Mulliken, J.
;
Guttmacher, A.
;
Wilroy, R.
;
Clarke, L.
;
Hollway, G.
;
Ades, L.
;
Haan, E.
;
Mulley, J.
;
Cohen, M.
;
et al.
2007
The Women's international study of long-duration oestrogen after menopause (WISDOM): a randomised controlled trial
Vickers, M.
;
Martin, J.
;
Meade, T.
;
Wilkes, H.
;
Ford, D.
;
Walgrove, A.
;
Arasaratnum, N.
;
Collins, N.
;
Furness, P.
;
Ghali, M.
;
Gordon, E.
;
Huppert, F.
;
Islam, Z.
;
Knott, C.
;
Meredith, S.
;
Prince, M.
;
Purdon, S.
;
Richards, M.
;
Taylor, L.
;
Welton, A.
;
et al.
2007
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitus
Raymond, F.
;
Tarpey, P.
;
Edkins, S.
;
Tofts, C.
;
O'Meara, S.
;
Teague, J.
;
Butler, A.
;
Stevens, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Dicks, E.
;
Gray, K.
;
Harrison, R.
;
Hills, K.
;
Hinton, J.
;
Jones, D.
;
Menzies, A.
;
Perry, J.
;
Raine, K.
;
et al.
2018
The impact of the 13 valent conjugate pneumococcal vaccine on pneumococcal serotypes causing childhood empyema in Australia
Strachan, R.
;
Beggs, S.
;
Fearon, D.
;
Gilbert, G.
;
Homaira, N.
;
Lambert, S.
;
Marshall, H.
;
Martin, A.
;
McCallum, G.
;
McCullagh, A.
;
McDonald, T.
;
Mcintyre, P.
;
Oftadeh, S.
;
Ranganathan, S.
;
Suresh, S.
;
Teoh, L.
;
Twaij, A.
;
Wainwright, C.
;
Wong, M.
;
Snelling, T.
;
et al.
;
The Australia & New Zealand Society of Respiratory Science and The Thoracic Society of Australia and New Zealand (ANZSRS/TSANZ) Annual Scientific Meeting 2018 (23 Mar 2018 - 27 Mar 2018 : Adelaide, AUSTRALIA)
2014
The inherited cancer connect (iccon) mutation-carrier database
James, P.A.
;
Petelin, L.
;
Campbell, I.
;
Dawkins, H.
;
Fox, S.
;
Hiller, J.
;
Kirk, J.
;
Lindeman, G.
;
Macrae, F.
;
Mascarenhas, L.
;
McGaughran, J.
;
Meiser, B.
;
Morrow, A.
;
Nichols, C.
;
Pachter, N.
;
Saunders, C.
;
Scott, C.
;
Poplawski, N.
;
Thrupp, L.
;
Trainer, A.
;
et al.
;
COSA's 41st Annual Scientific Meeting. Joining Forces - Accelerating Progress (2 Dec 2014 - 4 Dec 2014 : Melbourne, Vic.)
2020
Septum resection in women with a septate uterus: a cohort study
Rikken, J.F.
;
Verhorstert, K.W.
;
Emanuel, M.H.
;
Kuchenbecker, W.K.
;
Jansen, F.W.
;
Torrenga, B.
;
Schols, W.A.
;
Verhoeve, H.R.
;
Hoek, A.
;
Clark, T.J.
;
Stephenson, M.
;
Mol, B.W.
;
Van der Veen, F.
;
Van Wely, M.
;
Goddijn, M.
;
Bongers, M.Y.
;
van der Steeg, J.W.
;
Janssen, I.A.H.
;
Kapiteijn, K.
;
Torrance, H.L.
;
et al.
2019
Septum resection in women with a septate uterus: a cohort study
Rikken, J.F.
;
Verhorstert, K.W.
;
Emanuel, M.H.
;
Kuchenbecker, W.K.
;
Jansen, F.W.
;
Torrenga, B.
;
Schols, W.A.
;
Verhoeve, H.R.
;
Hoek, A.
;
Clark, T.J.
;
Stephenson, M.
;
Mol, B.W.
;
Van der Veen, F.
;
Van Wely, M.
;
Goddijn, M.
;
Bongers, M.Y.
;
van der Steeg, J.W.
;
Janssen, I.A.H.
;
Kapiteijn, K.
;
Torrance, H.L.
;
et al.
;
Annual Meeting of the European Society of Human Reproduction and Embryology (ESHRE) (24 Jun 2019 - 26 Jun 2019 : Vienna, AUSTRIA)
Discover
Author
21
Porath, M.
19
Bloemenkamp, K.
14
Gecz, J.
12
Mol, B.
12
Papatsonis, D.
10
Tarpey, P.
10
Van Esch, H.
9
Corbett, M.
9
Field, M.
9
Franssen, M.
.
next >
Subject
92
Humans
65
Female
45
Male
29
Adult
27
Mutation
25
Pedigree
22
Pregnancy
21
Child
16
Adolescent
16
Molecular Sequence Data
.
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Date issued
30
2020 - 2024
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2010 - 2019
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2000 - 2009
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1995 - 1999