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Results 31-40 of 54 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
1997
Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat
Yu, S.
;
Mangelsdorf, M.
;
Hewett, D.
;
Hobson, L.
;
Baker, E.
;
Eyre, H.
;
Lapsys, N.
;
Le Paslier, D.
;
Doggett, N.
;
Sutherland, G.
;
Richards, R.
1996
Positional cloning of the Fanconi anaemia group A gene
Apostolou, S.
;
Whitmore, S.
;
Crawford, J.
;
Lennon, G.
;
Sutherland, G.
;
Callen, D.
;
Ianzano, L.
;
Savino, M.
;
d'Apolito, M.
;
Notarangelo, A.
;
Memeo, E.
;
Piemontese, M.
;
Zelante, L.
;
Savoia, A.
;
Gibson, R.
;
Tipping, A.
;
Morgan, N.
;
Hassock, S.
;
Jansen, S.
;
de Ravel, T.
;
et al.
1995
Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndrome
Scott, H.
;
Blanch, L.
;
Guo, X.H.
;
Freeman, C.
;
Orsborn, A.
;
Baker, E.
;
Sutherland, G.
;
Morris, C.
;
Hopwood, J.
1998
FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis
Hewett, D.
;
Handt, O.
;
Hobson, L.
;
Mangelsdorf, M.
;
Eyre, H.
;
Baker, E.
;
Sutherland, G.
;
Schuffenhauer, S.
;
Mao, J.I.
;
Richards, R.
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.
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.
1995
Molecular cloning of the cDNA encoding human skeletal muscle triadin and its localisation to chromosome 6q22-6q23
Taske, N.
;
Eyre, H.
;
O'Brien, R.
;
Sutherland, G.
;
Denborough, M.
;
Foster, P.
1995
Assignment of the human pyruvate carboxylase gene (PC) to 11q13.4 by fluorescence in situ hybridisation
Walker, M.
;
Baker, E.
;
Wallace, J.
;
Sutherland, G.
1999
Genomic structure and expression analysis of the spastic paraplegia gene, SPG7
Settasatian, C.
;
Whitmore, S.
;
Crawford, J.
;
Bilton, R.
;
Cleton-Jansen, A.M.
;
Sutherland, G.
;
Callen, D.
Discover
Author
19
Eyre, H.
14
Baker, E.
7
Crawford, J.
7
Nicholl, J.
6
Mulley, J.
5
Callen, D.
5
Gecz, J.
4
Richards, R.
4
Woollatt, E.
3
Copeland, N.
.
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Subject
52
Humans
51
Molecular Sequence Data
33
Chromosome Mapping
30
Amino Acid Sequence
28
Animals
23
Cloning, Molecular
20
In Situ Hybridization, Fluorescence
18
Mice
17
DNA, Complementary
17
Male
.
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Date issued
2
2004
1
2003
1
2002
7
2001
2
2000
10
1999
3
1998
7
1997
8
1996
13
1995
.
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