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Results 11-20 of 25 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
1995
The CEPH consortium linkage map of human chromosome 16
Kozman, H.
;
Keith, T.
;
Donis-Keller, H.
;
White, R.
;
Weissenbach, J.
;
Sutherland, G.
1997
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies
D'Adamo, P.
;
Fassone, L.
;
Gedeon, A.
;
Janssen, E.
;
Bione, S.
;
Bolhuis, P.
;
Barth, P.
;
Wilson, M.
;
Haan, E.
;
Orstavik, H.
;
Patton, M.
;
Green, A.
;
Zammarchi, E.
;
Donati, M.
;
Toniolo, D.
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.
1997
AMP-activated protein kinase isoenzyme family: subunit structure and chromosomal location
Stapleton, D.
;
Woollatt, E.
;
Mitchelhill, K.
;
Nicholl, J.
;
Fernandez, C.
;
Michell, B.
;
Witters, L.
;
Power, D.
;
Sutherland, G.
;
Kemp, B.
1995
A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy
Laing, N.
;
Wilton, S.
;
Akkari, P.
;
Dorosz, S.
;
Boundy, K.
;
Kneebone, C.
;
Blumbergs, P.
;
White, S.
;
Watkins, H.
;
Love, D.
;
Haan, E.
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.
1998
Preferential pre-mRNA utilisation of an upstream cryptic 5' splice site created by a single base deletion mutation in exon 37 of the FBN-1 gene
Gibson, M.
;
Ellis, S.
;
Ades, L.
;
Haan, E.
;
Cleary, E.
1998
Characterization and chromosome location of the gene GSTZ1 encoding the human Zeta class glutathione transferase and maleylacetoacetate isomerase
Blackburn, A.
;
Woollatt, E.
;
Sutherland, G.
;
Board, P.
Discover
Author
16
Sutherland, G.
7
Baker, E.
5
Eyre, H.
5
Haan, E.
3
Akkari, P.
3
Callen, D.
3
Laing, N.
3
Nicholl, J.
3
Richards, R.
3
Wilton, S.
.
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Subject
25
Humans
17
Base Sequence
14
Chromosome Mapping
12
Amino Acid Sequence
12
Animals
10
Female
9
DNA Primers
9
In Situ Hybridization, Fluorescence
8
Sequence Homology, Amino Acid
7
Polymerase Chain Reaction
.
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Date issued
1
1999
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1998
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1997
5
1996
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1995