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Preview	Issue Date	Title	Author(s)
	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.
	2002	CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3	Kochetkova, M.; McKenzie, O.; Bais, A.; Martin, J.; Secker, G.; Seshadri, R.; Powell, J.; Hinze, S.; Gardner, A.; Spendlove, H.; O'Callaghan, N.; Cleton-Jansen, A.; Cornelisse, C.; Whitmore, S.; Crawford, J.; Kremmidiotis, G.; Sutherland, G.; Callen, D.
	2004	Aberrant CBFA2T3B gene promoter methylation in breast tumors	Bais, A.; Gardner, A.; McKenzie, O.; Callen, D.; Sutherland, G.; Kremmidiotis, G.
	1999	The Batten disease gene product (CLN3p) is a Golgi integral membrane protein	Kremmidiotis, G.; Lensink, I.; Bilton, R.; Woollatt, E.; Chataway, T.; Sutherland, G.; Callen, D.
	1995	Paracentric inversions do not normally generate monocentric recombinant chromosomes	Sutherland, G.; Callen, D.; McKinlay Gardner, R.
	2002	Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies	Baker, E.; Hinton, L.; Callen, D.; Altree, M.; Dobbie, A.; Eyre, H.; Sutherland, G.; Thompson, E.; Thompson, P.; Woollatt, E.; Haan, E.
	1999	C160rf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain	Bhalla, K.; Eyre, H.; Whitmore, S.; Sutherland, G.; Callen, D.
	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.
	1995	Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a 'hot-spot' for recombination at 16p12	Callen, D.; Lane, S.; Kozman, H.; Kremmidiotis, G.; Whitmore, S.; Lowenstein, M.; Doggett, N.; Kenmochi, N.; Page, D.; Maglott, D.; Nierman, W.; Murakawa, K.; Sikela, J.; Houlgatte, R.; Auffray, C.; Sutherland, G.
	1998	Construction of a high-resolution physical and transcription map of chromosome 16q24.3 - a region of frequent loss of heterozygosity in sporadic breast cancer	Whitmore, S.; Crawford, J.; Apostolou, S.; Eyre, H.; Baker, E.; Lower, K.; Settasatian, C.; Goldup, S.; Seshadri, R.; Gibson, R.; Mathew, C.; Cleton-Jansen, A.M.; Savoia, A.; Pronk, J.; Auerbach, A.; Doggett, N.; Sutherland, G.; Callen, D.