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Preview	Issue Date	Title	Author(s)
	1996	Characterisation of four novel fibrillin-1 mutations in the Marfan syndrome	Ades, L.; Haan, E.; Colley, A.; Richards, R.
	1995	Prenatal exposure to phenytoin, facial development and a possible role for vitamin K	Howe, A.; Lipson, A.; Sheffield, L.; Haan, E.; Halliday, J.; Jensen, F.; David, D.; Webster, W.
	1995	Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome	Ades, L.; Morris, L.; Power, R.; Wilson, M.; Haan, E.; Bateman, J.; Milewicz, D.; Sillence, D.
	1997	First-trimester diagnosis of Smith-Lemli-Opitz syndrome	Sharp, P.; Haan, E.; Fletcher, J.; Khong, T.; Carey, W.
	1997	Mutation detection in FGFR2 craniosynostosis syndromes	Hollway, G.; Suthers, G.; Haan, E.; Thompson, E.; David, D.; Gecz, J.; Mulley, J.
	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.
	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.