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Issue Date
Title
Author(s)
1996
FRAGILE X SYNDROME AND FRAGILE XE MENTAL RETARDATION [Review]
Sutherland, G.
;
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
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
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.
1996
Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21
Wallace, R.
;
Berkovic, S.
;
Howell, R.
;
Sutherland, G.
;
Mulley, J.
Discover
Author
1
Hollway, G.
1
Howell, R.
1
Oostra, B.
1
Propping, P.
1
Steinlein, O.
1
Turner, G.
.
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4
Female
4
Humans
4
Male
2
Base Sequence
2
Chromosomes, Human, Pair 20
2
DNA Primers
2
Epilepsy, Frontal Lobe
2
Fragile X Syndrome
2
Genetic Carrier Screening
2
Genetic Linkage
.
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1997
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1996
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1995