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Issue Date
Title
Author(s)
1995
Fragile X syndrome and other dynamic mutation diseases
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.
1999
Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndrome
Singh, R.
;
Sutherland, G.
;
Manson, J.
Discover
Author
2
Berkovic, S.
2
Mulley, J.
2
Phillips, H.
2
Richards, R.
2
Scheffer, I.
1
Baker, E.
1
Hollway, G.
1
Jones, C.
1
Langdon, W.
1
Manson, J.
.
next >
Subject
5
Humans
4
Male
2
Animals
2
Base Sequence
2
Chromosomes, Human, Pair 20
2
Epilepsy, Frontal Lobe
2
Fragile X Syndrome
2
Genetic Linkage
2
Molecular Sequence Data
2
Receptors, Nicotinic
.
next >
Date issued
1
1999
4
1995