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Results 21-30 of 39 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2000
The clinical significance of fragile sites on human chromosomes
Sutherland, G.
;
Baker, E.
2004
Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein
Sarafidou, T.
;
Kahl, C.
;
Martinez-Garay, I.
;
Mangelsdorf, M.
;
Gesk, S.
;
Baker, E.
;
Kokkinaki, M.
;
Talley, P.
;
Maltby, E.
;
French, L.
;
Harder, L.
;
Hinzmann, B.
;
Nobile, C.
;
Richkind, K.
;
Finnis, M.
;
Deloukas, P.
;
Sutherland, G.
;
Kutsche, K.
;
Moschonas, N.
;
Siebert, R.
;
et al.
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.
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.
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.
2003
Forgotten fragile sites and related phenomena
Sutherland, G.
;
Baker, E.
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.
1997
Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal disease
Narahara, K.
;
Baker, E.
;
Ito, S.
;
Yokoyama, Y.
;
Yu, S.
;
Hewitt, D.
;
Sutherland, G.
;
Eccles, M.
;
Richards, R.
Discover
Author
8
Eyre, H.
5
Richards, R.
4
Schofield, P.
4
Yu, S.
3
Callen, D.
3
Crawford, J.
3
Doggett, N.
3
Haan, E.
3
Mangelsdorf, M.
3
Townsend-Nicholson, A.
.
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Subject
31
Humans
19
Molecular Sequence Data
17
Chromosome Mapping
17
In Situ Hybridization, Fluorescence
14
Base Sequence
12
Animals
12
Male
10
Amino Acid Sequence
10
Cloning, Molecular
9
Chromosome Fragile Sites
.
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2004
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2002
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2001
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2000
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1999
4
1998
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1997
7
1996
14
1995
.
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