1. Adelaide Research & Scholarship

Browsing "Genetics publications" by Author Eyre, H.

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Showing results 1 to 8 of 8
PreviewIssue DateTitleAuthor(s)
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.
1999Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardationGecz, J.; Barnett, S.; Liu, J.; Hollway, G.; Donnelly, A.; Eyre, H.; Eshkevari, H.; Baltazar, R.; Grunn, A.; Nagaraja, R.; Gilliam, C.; Peltonen, L.; Sutherland, G.; Baron, M.; Mulley, J.
1997High resolution characterisation of an interstitial deletion of less than 1.9Mb at 4p16.3 associated with Wolf-Hirschhorn SyndromeFang, Y.; Bain, S.; Haan, E.; Eyre, H.; MacDonald, M.; Wright, T.; Altherr, M.; Riess, O.; Sutherland, G.; Callen, D.
2011Identification of SOX3 as an XX male sex reversal gene in mice and humansSutton, E.; Hughes, J.; White, S.; Sekido, R.; Tan, J.; Arboleda, V.; Rogers, N.; Knower, K.; Rowley, L.; Eyre, H.; Rizzoti, K.; McAninch, D.; Golcalves, J.; Slee, J.; Turbitt, E.; Bruno, D.; Bengtsson, H.; Harley, V.; Vilain, E.; Sinclair, A.; et al.
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.
1997Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogeneticsCallen, D.; Yip, M.Y.; Eyre, H.
1998The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.Kortschak, R.; Reimann, H.; Zimmer, M.; Eyre, H.; Saint, R.; Jenne, D.
1998The identification and localisation of a human gene with sequence similarity to Polycomblike of Drosophila melanogasterCoulson, M.; Robert, S.; Eyre, H.; Saint, R.
Showing results 1 to 8 of 8