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Results 11-20 of 26 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
1996
Further characterization of proteins associated with elastic fiber microfibrils including the molecular cloning of MAGP-2 (MP25)
Gibson, M.
;
Hatzinikolas, G.
;
Kumaratilake, J.
;
Sandberg, L.
;
Nicholl, J.
;
Sutherland, G.
;
Cleary, E.
2003
Disruption of the Serine/Threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation
Kalscheuer, V.
;
Tao, J.
;
Donnelly, A.
;
Hollway, G.
;
Schwinger, E.
;
Kubart, S.
;
Menzel, C.
;
Hoeltzenbein, M.
;
Tommerup, N.
;
Eyre, H.
;
Harbord, M.
;
Haan, E.
;
Sutherland, G.
;
Ropers, H.
;
Gecz, J.
2004
GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies
Dibbens, L.
;
Feng, H.
;
Richards, M.
;
Harkin, L.
;
Hodgson, B.
;
Scott, D.
;
Jenkins, M.
;
Petrou, S.
;
Sutherland, G.
;
Scheffer, I.
;
Berkovic, S.
;
Mcdonald, R.
;
Mulley, J.
1997
FMR2 expression in families with FRAXE mental retardation
Gecz, J.
;
Oostra, B.
;
Hockey, A.
;
Carbonell, P.
;
Turner, G.
;
Haan, E.
;
Sutherland, G.
;
Mulley, J.
1995
Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus
Nancarrow, J.
;
Holman, K.
;
Hori, T.
;
Denton, M.
;
Sutherland, G.
;
Richards, R.
1995
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to 20q13.2
Phillips, H.
;
Scheffer, I.
;
Berkovic, S.
;
Hollway, G.
;
Sutherland, G.
;
Mulley, J.
1995
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2
Jones, C.
;
Penny, L.
;
Mattina, T.
;
Yu, S.
;
Baker, E.
;
Voullaire, L.
;
Langdon, W.
;
Sutherland, G.
;
Richards, R.
;
Tunnacliffe, A.
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.
2005
Frequency of truly cryptic subtelomere abnormalities - a study of 534 patients and literature review
Yu, S.
;
Baker, E.
;
Hinton, L.
;
Eyre, H.
;
Waters, W.
;
Higgins, S.
;
Sutherland, G.
;
Haan, E.
2007
NEDD4-2 as a potential candidate susceptibility gene for epileptic photosensitivity
Dibbens, L.
;
Ekberg, J.
;
Taylor, I.
;
Hodgson, B.
;
Conroy, S.
;
Lensink, I.
;
Kumar, S.
;
Zielinski, M.
;
Harkin, L.
;
Sutherland, G.
;
Adams, D.
;
Berkovic, S.
;
Scheffer, I.
;
Mulley, J.
;
Poronnik, P.
Discover
Author
7
Eyre, H.
7
Mulley, J.
6
Baker, E.
5
Berkovic, S.
5
Haan, E.
5
Scheffer, I.
4
Copeland, N.
4
Crawford, J.
4
Jenkins, N.
3
Callen, D.
.
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Subject
26
Humans
21
Male
11
Chromosome Mapping
10
Base Sequence
10
Molecular Sequence Data
9
Animals
8
Pedigree
6
Amino Acid Sequence
5
In Situ Hybridization, Fluorescence
5
Intellectual Disability
.
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Date issued
1
2010 - 2011
9
2000 - 2009
16
1995 - 1999