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Preview	Issue Date	Title	Author(s)
	2000	New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndrome	Cox, T.; Allen, L.; Cox, L.; Hopwood, B.; Goodwin, B.; Haan, E.; Suthers, G.
	2006	FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited	Ades, L.; Sullivan, K.; Biggin, A.; Haan, E.; Brett, M.; Holman, K.; Dixon, J.; Robertson, S.; Holmes, A.; Rogers, J.; Bennetts, B.
	2001	Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome	Kelberman, D.; Tyson, J.; Chandler, D.; McInerney, A.; Slee, J.; Albert, D.; Aymat, A.; Botma, M.; Calvert, M.; Goldblatt, J.; Haan, E.; Laing, N.; Lim, J.; Malcolm, S.; Singer, S.; Winter, R.; Bitner-Glindzicz, M.
	1998	SHORT syndrome: distinctive radiographic features	Haan, E.; Morris, L.
	1997	The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies	D'Adamo, P.; Fassone, L.; Gedeon, A.; Janssen, E.; Bione, S.; Bolhuis, P.; Barth, P.; Wilson, M.; Haan, E.; Orstavik, H.; Patton, M.; Green, A.; Zammarchi, E.; Donati, M.; Toniolo, D.
	2008	Ocular colobomata, polydactyly, cleft palate and panhypopituitarism: a new syndrome	Laforest, C.; Leibovitch, I.; Selva-Nayagam, D.; Crompton, J.; Haan, E.
	2005	The Hunter-McAlpine syndrome results from duplication 5q35-qter	Hunter, A.; DuPont, B.; McLaughlin, M.; Hinton, L.; Baker, E.; Ades, L.; Haan, E.; Schwartz, C.
	1995	Hydrometrocolpos and segmental colonic dilatation in a girl with megacystis-microcolon-intestinal hypoperistalsis syndrome	Dewan, P.; Brown, N.; Murthy, D.; Dnaga-Christian, B.; Haan, E.; Byard, R.; Watters, D.