Skip navigation
Home
Browse
Communities
& Collections
Browse Items by:
Issue Date
Author
Title
Advisor
Help
Sign on to:
My DSpace
Receive email
updates
Edit Profile
Adelaide Research & Scholarship
Adelaide Research & Scholarship
Search
Search:
All collections
Schools and Disciplines
School of Paediatrics & Reproductive Health
Paediatrics
Paediatrics publications
for
Current filters:
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Start a new search
Add filters:
Use filters to refine the search results.
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Results 61-70 of 233 (Search time: 0.003 seconds).
previous
1
...
4
5
6
7
8
9
10
...
24
next
Item hits:
Preview
Issue Date
Title
Author(s)
2009
In Vitro Differentiation of Human Calvarial Suture Derived Cells With and Without Dexamethasione Does Not Induce In Vivo-Like Expression
Coussens, A.
;
Hughes, I.
;
Morris, C.
;
Powell, B.
;
Anderson, P.
2006
FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited
Ades, L.
;
Sullivan, K.
;
Biggin, A.
;
Haan, E.
;
Brett, M.
;
Holman, K.
;
Dixon, J.
;
Robertson, S.
;
Holmes, A.
;
Rogers, J.
;
Bennetts, B.
2004
Identification of a SEDL gene mutation in an individual with Leber hereditary optic neuropathy and spondyloepiphyseal dysplasia
Shaw, M.
;
Gecz, J.
;
McDonough, B.
;
Hodess, A.
;
Harter, D.
2007
Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX Consortium
de Brouwer, A.
;
Yntema, H.
;
Kleefstra, T.
;
Lugtenberg, D.
;
Oudakker, A.
;
de Vries, B.
;
van Bokhoven, H.
;
Van Esch, H.
;
Frints, S.
;
Froyen, G.
;
Fryns, J.
;
Raynaud, M.
;
Moizard, M.
;
Ronce, N.
;
Bensalem, A.
;
Moraine, C.
;
Poirier, K.
;
Castelnau, L.
;
Saillour, Y.
;
Bienvenu, T.
;
et al.
2006
HOXD10 M319K mutation in a family with isolated congenital vertical Talus
Dobbs, M.
;
Gurnett, C.
;
Pierce, B.
;
Exner, G.
;
Robarge, J.
;
Morcuende, J.
;
Cole, W.
;
Templeton, P.
;
Foster, B.
;
Bowcock, A.
2005
Unstable Robertsonian translocations der(13;15)(q10;q10): Heritable chromosome fission without phenotypic effect in two kindreds
Perry, J.
;
White, S.
;
Nouri, S.
;
Bain, S.
;
Hutchinson, R.
;
La, P.
;
Northrop, E.
;
Eyre, H.
;
Pertile, M.
;
Hocking, T.
;
Thompson, E.
;
Yu, S.
;
Choo, K.
;
Slater, H.
2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutations
Baker, N.
;
Morgelin, M.
;
Pace, R.
;
Peat, R.
;
Adams, N.
;
Gardner, R.
;
Rowland, L.
;
Miller, G.
;
De Jonghe, P.
;
Ceulemans, B.
;
Hannibal, M.
;
Edwards, M.
;
Thompson, E.
;
Jacobson, R.
;
Quinlivan, R.
;
Aftimos, S.
;
Kornberg, A.
;
North, K.
;
Bateman, J.
;
Lamande, S.
2002
The molecular basis of cystathionine b-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatment
Gaustadnes, M.
;
Wilcken, B.
;
Oliveriusova, J.
;
McGill, J.
;
Fletcher, J.
;
Kraus, J.
;
Wilcken, D.
2008
Higher dose of docosahexaenoic acid in the neonatal period improves visual acuity of preterm infants: results of a randomized controlled trial
Smithers, L.
;
Gibson, R.
;
McPhee, A.
;
Makrides, M.
2006
A pilot study of the safety implications of Australian nurses' sleep and work hours
Dorrian, J.
;
Lamond, N.
;
van den Heuvel, C.
;
Pincombe, J.
;
Rogers, A.
;
Drew, D.
Discover
Author
29
Gecz, J.
22
Davidson, G.
16
et al.
15
Haan, E.
14
Omari, T.
13
Baghurst, P.
12
Couper, J.
12
Hopwood, J.
11
Sawyer, M.
11
Scheffer, I.
.
next >
Subject
191
Female
80
Child
75
Adult
73
Adolescent
62
Child, Preschool
59
Infant
48
Infant, Newborn
43
Pedigree
40
Middle Aged
39
Mutation
.
next >
Date issued
27
2009
31
2008
29
2007
15
2006
29
2005
20
2004
26
2003
15
2002
16
2001
25
2000
.
next >