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Results 1-10 of 15 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2003
Two further cases of Ohdo syndrome delineate the phenotypic variability of the condition
White, S.
;
Ades, L.
;
Amor, D.
;
Liebelt, J.
;
Bankier, A.
;
Baker, E.
;
Wilson, M.
;
Savarirayan, R.
2003
Transfer of chromosome 8 into two breast cancer cell lines: total exclusion of three regions indicates location of putative in vitro growth suppressor genes
Wilson, P.
;
Cuthbert, A.
;
Marsh, A.
;
Arnold, J.
;
Flanagan, J.
;
Mulford, C.
;
Trott, D.
;
Baker, E.
;
Purdie, D.
;
Newbold, R.
;
Chenevix-Trench, G.
2010
The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletion
MacKinnon, R.
;
Selan, C.
;
Wall, M.
;
Baker, E.
;
Nandurkar, H.
;
Campbell, L.
2000
Peek-a-boo fragile sites? Not really
Sutherland, G.
;
Baker, E.
2000
The clinical significance of fragile sites on human chromosomes
Sutherland, G.
;
Baker, E.
2000
Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells
Ried, K.
;
Finnis, M.
;
Hobson, L.
;
Mangelsdorf, M.
;
Dayan, S.
;
Nancarrow, J.
;
Woollatt, E.
;
Kremmidiotis, G.
;
Gardner, A.
;
Venter, D.
;
Baker, E.
;
Richards, R.
2002
Defining regions of loss of heterozygosity of 16q in breast cancer cell lines
Callen, D.
;
Crawford, J.
;
Derwas, C.
;
Cleton-Jansen, A.
;
Cornelisse, C.
;
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.
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.
2005
The Hunter-McAlpine syndrome results from duplication 5q35-qter
Hunter, A.
;
DuPont, B.
;
McLaughlin, M.
;
Hinton, L.
;
Baker, E.
;
Ades, L.
;
Haan, E.
;
Schwartz, C.
Discover
Author
8
Sutherland, G.
3
Crawford, J.
2
Ades, L.
2
Callen, D.
2
Eyre, H.
2
Finnis, M.
2
Gardner, A.
2
Haan, E.
2
Hinton, L.
2
Kremmidiotis, G.
.
next >
Subject
7
Female
6
Male
5
Chromosome Fragile Sites
4
Alternative Splicing
4
Chromosome Aberrations
4
Chromosome Fragility
4
Chromosomes, Human, Pair 16
4
In Situ Hybridization, Fluorescence
4
Intellectual Disability
4
Molecular Sequence Data
.
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2003
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2002
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2000