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Issue Date
Title
Author(s)
2005
Common chromosomal fragile site FRA16D mutation in cancer cells
Finnis, M.
;
Dayan, S.
;
Hobson, L.
;
Chenevix-Trench, G.
;
Friend, K.
;
Ried, K.
;
Venter, D.
;
Woollatt, E.
;
Baker, E.
;
Richards, R.
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.
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.
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.
Discover
Author
4
Hobson, L.
3
Mangelsdorf, M.
3
Sutherland, G.
2
Dayan, S.
2
Eyre, H.
2
Finnis, M.
2
Hewett, D.
2
Ried, K.
2
Venter, D.
2
Woollatt, E.
.
next >
Subject
5
Chromosome Fragile Sites
5
Humans
4
Base Sequence
4
Chromosome Fragility
3
Chromosomes, Human, Pair 16
3
Repetitive Sequences, Nucleic Acid
2
Blotting, Southern
2
Chromosome Deletion
2
Cloning, Molecular
2
DNA, Satellite
.
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