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Results 1-6 of 6 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1997
High resolution characterisation of an interstitial deletion of less than 1.9Mb at 4p16.3 associated with Wolf-Hirschhorn Syndrome
Fang, Y.
;
Bain, S.
;
Haan, E.
;
Eyre, H.
;
MacDonald, M.
;
Wright, T.
;
Altherr, M.
;
Riess, O.
;
Sutherland, G.
;
Callen, D.
1997
Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogenetics
Callen, D.
;
Yip, M.Y.
;
Eyre, H.
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
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.
Town, M.
;
Jean, G.
;
Cherqui, S.
;
Attard, M.
;
Forestier, L.
;
Whitmore, S.
;
Callen, D.
;
Gribouval, O.
;
Broyer, M.
;
Bates, G.
;
van't Hoff, W.
;
Antignac, C.
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
ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, & is shown to be expressed in primitive hematopoietic precursors.
Kuss, B.
;
O'Neill, G.
;
Eyre, H.
;
Doggett, N.
;
Callen, D.
;
Davey, R.
Discover
Author
1
Broyer, M.
1
Cavanaugh, J.
1
Cherqui, S.
1
Davey, R.
1
Doggett, N.
1
Fang, Y.
1
Foote, S.
1
Forestier, L.
1
Gorska, M.
1
Gribouval, O.
.
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Subject
6
Humans
4
Chromosome Mapping
4
In Situ Hybridization, Fluorescence
3
Chromosomes, Human, Pair 16
3
Gene Deletion
2
Cloning, Molecular
2
Genetic Markers
2
Karyotyping
2
Pedigree
2
Sequence Homology, Amino Acid
.
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Date issued
4
1998
2
1997