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Issue Date
Title
Author(s)
1999
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3
Cleton-Jansen, A.M.
;
Moerland, E.
;
Pronk, J.
;
Van Berkel, C.
;
Apostolou, S.
;
Crawford, J.
;
Savoia, A.
;
Auerbach, A.
;
Callen, D.
;
Cornelisse, C.
1998
Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16
Cavanaugh, J.
;
Callen, D.
;
Wilson, S.
;
Stanford, P.
;
Sraml, M.
;
Gorska, M.
;
Crawford, J.
;
Whitmore, S.
;
Shlegel, C.
;
Foote, S.
;
Kohonen-Corish, M.
;
Pavli, P.
1998
Localisation of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity.
Kremmidiotis, G.
;
Baker, E.
;
Crawford, J.
;
Eyre, H.
;
Nahmias, J.
;
Callen, D.
1998
Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer
Whitmore, S.
;
Settasatian, C.
;
Crawford, J.
;
Lower, K.
;
McCallum, B.
;
Seshadri, R.
;
Cornelisse, C.
;
Moerland, E.
;
Cleton-Jansen, A.M.
;
Tipping, A.
;
Mathew, C.
;
Savnio, M.
;
Savoia, A.
;
Verlander, P.
;
Auerbach, A.
;
Van Berkel, C.
;
Pronk, J.
;
Doggett, N.
;
Callen, D.
1999
The PISSLRE Gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer
Crawford, J.
;
Ianzano, L.
;
Savino, M.
;
Whitmore, S.
;
Cleton-Jansen, A.M.
;
Settasatian, C.
;
d'Apolito, M.
;
Seshadri, R.
;
Pronk, J.
;
Auerbach, A.
;
Verlander, P.
;
Mathew, C.
;
Tipping, A.
;
Doggett, N.
;
Zelante, L.
;
Callen, D.
;
Savoia, A.
Discover
Author
3
Auerbach, A.
3
Cleton-Jansen, A.M.
3
Pronk, J.
3
Savoia, A.
3
Whitmore, S.
2
Cornelisse, C.
2
Doggett, N.
2
Mathew, C.
2
Moerland, E.
2
Seshadri, R.
.
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Subject
1
Cloning, Molecular
1
Crohn Disease
1
Cyclin-Dependent Kinases
1
Cytoskeletal Proteins
1
DNA Mutational Analysis
1
DNA Primers
1
DNA-Binding Proteins
1
Exons
1
Fanconi Anemia Complementation Gr...
1
Gene Amplification
.
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Date issued
2
1999
3
1998