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Preview	Issue Date	Title	Author(s)
	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.
	1999	Analysis of five Duchenne muscular dystrophy exons and gender determination using conventional duplex polymerase chain reaction on single cells	Hussey, N.; Donggui, H.; Froiland, D.; Hussey, D.; Haan, E.; Matthews, C.; Craig, J.
	1998	Autosomal dominant Klippel-Feil anomaly with cleft palate	Thompson, E.; Haan, E.; Sheffield, L.
	1998	SHORT syndrome: distinctive radiographic features	Haan, E.; Morris, L.
	2012	CCDC22: a novel candidate gene for syndromic X-linked intellectual disability	Voineagu, J.; Huang, L.; Winden, K.; Lazaro, M.; Haan, E.; Nelson, J.; McGaughran, J.; Nguyen, L.; Friend, K.; Hackett, A.; Field, M.; Gecz, J.; Geschwind, D.
	1999	X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation	Woffendin, H.; Jakins, T.; Jouet, M.; Stewart, H.; Landy, S.; Haan, E.; Harris, A.; Donnai, D.; Read, A.; Kenwrick, S.
	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.
	1997	FMR2 expression in families with FRAXE mental retardation	Gecz, J.; Oostra, B.; Hockey, A.; Carbonell, P.; Turner, G.; Haan, E.; Sutherland, G.; Mulley, J.
	2008	Ocular colobomata, polydactyly, cleft palate and panhypopituitarism: a new syndrome	Laforest, C.; Leibovitch, I.; Selva-Nayagam, D.; Crompton, J.; Haan, E.
	2008	Pain characteristics and their association with quality of life and self-concept in children with hemiplegic cerebral palsy identified from a population register	Russo, R.; Miller, M.; Haan, E.; Cameron, I.; Crotty, M.