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Preview	Issue Date	Title	Author(s)
	1997	Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3	Mitchison, 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.
	2008	CBFA2T3-ZNF652 corepressor complex regulates transcription of the E-box gene HEB	Kumar, R.; Cheney, K.; McKirdy, R.; Neilsen, P.; Schulz, R.; Lee, J.; Cohen, J.; Booker, G.; Callen, D.
	2001	Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions	Cleton-Jansen, A.; Callen, D.; Seshadri, R.; Goldup, S.; McCallum, B.; Crawford, J.; Powell, J.; Settasatian, C.; van Beerendonk, H.; Moerland, E.; Smit, V.; Harris, W.; Millis, R.; Morgan, N.; Barnes, D.; Mathew, C.; Cornelisse, C.
	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.
	2006	ZNF652, a novel zinc finger protein, interacts with the putative breast tumor suppressor CBFA2T3 to repress transcription	Kumar, R.; Manning, J.; Spendlove, H.; Kremmidiotis, G.; McKirdy, R.; Lee, J.; Millband, D.; Cheney, K.; Stampfer, M.; Dwivedi, P.; Morris, H.; Callen, D.
	1997	Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogenetics	Callen, D.; Yip, M.Y.; Eyre, H.
	1998	Human 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.
	1998	Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2y: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene.	Schollen, E.; Pardon, E.; Heykants, L.; Renard, J.P.; Doggett, N.; Callen, D.; Cassiman, J.J.; Matthijs, G.
	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.
	2001	Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene	Bell, R.; Brice, G.; Child, A.; Murday, V.; Mansour, S.; Sandy, C.; Collin, J.; Brady, A.; Callen, D.; Burnand, K.; Mortimer, P.; Jeffery, S.