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Results 1-10 of 17 (Search time: 0.005 seconds).
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PreviewIssue DateTitleAuthor(s)
1997Assignment of the Human CC Chemokine Gene TARC (SCYA17) to chromosome 16q13Nomiyama, H.; Imai, T.; Kusuda, J.; Miura, R.; Callen, D.; Yoshie, O.
1999Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3Cleton-Jansen, A.; Moerland, E.; Pronk, J.; Van Berkel, C.; Apostolou, S.; Crawford, J.; Savoia, A.; Auerbach, A.; Callen, D.; Cornelisse, C.
1997Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogeneticsCallen, D.; Yip, M.; Eyre, H.
1998Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13.Nomiyama, H.; Imai, T.; Kusuda, J.; Miura, R.; Callen, D.; Yoshie, O.
1999The PISSLRE Gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancerCrawford, J.; Ianzano, L.; Savino, M.; Whitmore, S.; Cleton-Jansen, A.; 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.
1998ARA, 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.
1998Localisation of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels.Kalsi, G.; Whiting, P.; Bourdelles, B.; Callen, D.; Barnard, E.; Gurling, H.
1998Localisation 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.
1998Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancerWhitmore, S.; Settasatian, C.; Crawford, J.; Lower, K.; McCallum, B.; Seshadri, R.; Cornelisse, C.; Moerland, E.; Cleton-Jansen, A.; Tipping, A.; Mathew, C.; Savnio, M.; Savoia, A.; Verlander, P.; Auerbach, A.; Van Berkel, C.; Pronk, J.; Doggett, N.; Callen, D.
1998Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16Cavanaugh, J.; Callen, D.; Wilson, S.; Stanford, P.; Sraml, M.; Gorska, M.; Crawford, J.; Whitmore, S.; Shlegel, C.; Foote, S.; Kohonen-Corish, M.; Pavli, P.