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Results 21-26 of 26 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
1996
The first gene for an idiopathic epilepsy: A fruitful collaboration of Australian Clinical Research and Molecular Genetics
Berkovic, S.
;
Mulley, J.
2011
Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutations
Dibbens, L.
;
Kneen, R.
;
Bayly, M.
;
Heron, S.
;
Arsov, T.
;
Damiano, J.
;
Desai, T.
;
Gibbs, J.
;
McKenzie, F.
;
Mulley, J.
;
Ronan, A.
;
Scheffer, I.
1995
FRAXE and mental retardation
Mulley, J.
;
Yu, S.
;
Loesch, D.
;
Hay, D.
;
Donnelly, A.
;
Gedeon, A.
;
Carbonell, P.
;
Lopez, I.
;
Glover, G.
;
Garbarron, I.
;
Yu, P.
;
Baker, E.
;
Haan, E.
;
Hockey, A.
;
Knight, S.
;
Daview, K.
;
Richards, R.
;
Sutherland, G.
1998
PAK3 mutation in nonsyndromic X-linked mental retardation
Allen, K.
;
Gleeson, J.
;
Bagrodia, S.
;
Partington, M.
;
MacMillan, J.
;
Cerione, R.
;
Mulley, J.
;
Walsh, C.
1999
Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation
Gecz, J.
;
Barnett, S.
;
Liu, J.
;
Hollway, G.
;
Donnelly, A.
;
Eyre, H.
;
Eshkevari, H.
;
Baltazar, R.
;
Grunn, A.
;
Nagaraja, R.
;
Gilliam, C.
;
Peltonen, L.
;
Sutherland, G.
;
Baron, M.
;
Mulley, J.
1997
Gene structure and subcellular localisation of FMR2, a member of a new family of putative transcription activators
Gecz, J.
;
Bielby, S.
;
Sutherland, G.
;
Mulley, J.
Discover
Author
10
Gedeon, A.
8
Sutherland, G.
7
Donnelly, A.
6
Gecz, J.
4
Colley, A.
4
Phillips, H.
3
Baker, E.
3
Berkovic, S.
3
Haan, E.
3
Hollway, G.
.
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Subject
22
Humans
16
Male
15
Female
13
X Chromosome
11
Genetic Linkage
11
Intellectual Disability
10
Pedigree
9
Chromosome Mapping
8
Molecular Sequence Data
6
Genetic Markers
.
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Date issued
1
2010 - 2011
25
1995 - 1999