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Results 1-10 of 15 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1997Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3Mitchison, H.; Munroe, P.; O'Rawe, A.; Taschner, P.; De Vos, N.; Kremmidiotis, G.; Lensink, I.; Munk, A.; D'Arigo, K.; Anderson, J.; Lerner, T.; Moyzis, R.; Callen, D.; Breuning, M.; Doggett, N.; Gardiner, R.; Mole, S.
1995Mechanisms of small ring formation suggested by the molecular characterization of 2 small accessory ring chromosomes derived from chromosome 4Fang, Y.; Eyre, H.; Bohlander, S.; Estop, A.; McPherson, E.; Trager, T.; Riess, O.; Callen, D.
1999Origins of accessory small ring marker chromosomes derived from chromosome 1Callen, D.; Eyre, H.; Fang, Y.; Guan, X.; Veleba, A.; Martin, N.; McGill, J.; Haan, E.
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.
1995Assignment of the human skeletal muscle a-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridizationEyre, H.; Akkari, P.; Wilton, S.; Callen, D.; Baker, E.; Laing, N.
1999The Batten disease gene product (CLN3p) is a Golgi integral membrane proteinKremmidiotis, G.; Lensink, I.; Bilton, R.; Woollatt, E.; Chataway, T.; Sutherland, G.; Callen, D.
1995Paracentric inversions do not normally generate monocentric recombinant chromosomesSutherland, G.; Callen, D.; McKinlay Gardner, R.
1995Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisationHunt, C.; Eyre, H.; Akkari, P.; Meredith, C.; Dorosz, S.; Wilton, S.; Callen, D.; Laing, N.; Baker, E.
1995Localization of the gene for human 11b hydroxysteroid dehydrogenase type 2 enzyme to chromosome 16q22Krozowski, Z.; Baker, E.; Obeyesekere, V.; Callen, D.
1999C160rf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brainBhalla, K.; Eyre, H.; Whitmore, S.; Sutherland, G.; Callen, D.

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