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Results 21-29 of 29 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
1996
Identification of the gene FMR2, associated with FRAXE mental retardation
Gecz, J.
;
Gedeon, A.
;
Sutherland, G.
;
Mulley, J.
1995
A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
Steinlein, O.
;
Mulley, J.
;
Propping, P.
;
Wallace, R.
;
Phillips, H.
;
Sutherland, G.
;
Scheffer, I.
;
Berkovic, S.
1998
Polymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders.
Hollway, G.
;
Mulley, J.
1996
The first gene for an idiopathic epilepsy: A fruitful collaboration of Australian Clinical Research and Molecular Genetics
Berkovic, S.
;
Mulley, J.
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.
1999
Characterisation and expression of a large, 13.7 kb FMR2 isoform
Gecz, J.
;
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
Sutherland, G.
9
Gedeon, A.
8
Gecz, J.
6
Berkovic, S.
6
Donnelly, A.
6
Haan, E.
6
Hollway, G.
6
Phillips, H.
5
Scheffer, I.
4
Colley, A.
.
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Subject
21
Female
21
Male
14
Genetic Linkage
14
Pedigree
13
X Chromosome
11
Intellectual Disability
10
Chromosome Mapping
10
Molecular Sequence Data
9
Syndrome
8
Genetic Markers
.
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Date issued
4
1999
8
1998
4
1997
9
1996
4
1995