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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.
	1995	Mechanisms of small ring formation suggested by the molecular characterization of 2 small accessory ring chromosomes derived from chromosome 4	Fang, Y.; Eyre, H.; Bohlander, S.; Estop, A.; McPherson, E.; Trager, T.; Riess, O.; 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.
	1995	Assignment of the human skeletal muscle a-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization	Eyre, H.; Akkari, P.; Wilton, S.; Callen, D.; Baker, E.; Laing, N.
	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.
	1995	Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation	Hunt, C.; Eyre, H.; Akkari, P.; Meredith, C.; Dorosz, S.; Wilton, S.; Callen, D.; Laing, N.; Baker, E.
	1996	Molecular cloning of the cDNA and chromosome localization of the gene for human ubiquitin-conjugating enzyme 9	Wang, Z.; Qiu, Q.; Seufert, W.; Taguchi, T.; Testa, J.; Whitmore, S.; Callen, D.; Welsh, D.; Shenk, T.; Deuel, T.
	1996	Positional cloning of the Fanconi anaemia group A gene	Apostolou, S.; Whitmore, S.; Crawford, J.; Lennon, G.; Sutherland, G.; Callen, D.; Ianzano, L.; Savino, M.; d'Apolito, M.; Notarangelo, A.; Memeo, E.; Piemontese, M.; Zelante, L.; Savoia, A.; Gibson, R.; Tipping, A.; Morgan, N.; Hassock, S.; Jansen, S.; de Ravel, T.; et al.
	2004	The sequence and analysis of duplication-rich human chromosome 16	Martin, J.; Han, C.; Gordon, L.; Terry, A.; Prabhakar, S.; She, X.; Xie, G.; Hellsten, U.; Man, Y.; Altherr, M.; Couronne, O.; Aerts, A.; Bajorek, E.; Black, S.; Blumer, H.; Branscomb, E.; Brown, N.; Bruno, W.; Buckingham, J.; Callen, D.; et al.
	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.