Adelaide Research & Scholarship: Search

Search

Results 41-50 of 115 (Search time: 0.045 seconds).

previous
1
...
2
3
4
5
6
7
8
...
12
next

Item hits:

Preview	Issue Date	Title	Author(s)
	2016	Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID	van Bon, B.W.M.; Coe, B.P.; Bernier, R.; Green, C.; Gerdts, J.; Witherspoon, K.; Kleefstra, T.; Willemsen, M.H.; Kumar, R.; Bosco, P.; Fichera, M.; Li, D.; Amaral, D.; Cristofoli, F.; Peeters, H.; Haan, E.; Romano, C.; Mefford, H.C.; Scheffer, I.; Gecz, J.; et al.
	2013	Single-nucleotide polymorphism associations with preterm delivery: a case-control replication study and meta-analysis	O'Callaghan, M.; MacLennan, A.; McMichael, G.; Haan, E.; Dekker, G.
	2013	Genotype and clinical care correlations in craniosynostosis: Findings from a cohort of 630 australian and new zealand patients	Roscioli, T.; Haan, E.; Thompson, E.; David, D.; Anderson, P.
	2013	Rare copy number variation in cerebral palsy	McMichael, G.; Girirajan, S.; Moreno-De-Luca, A.; Gecz, J.; Shard, C.; Nguyen, L.; Nicholl, J.; Gibson, C.; Haan, E.; Eichler, E.; Martin, C.; MacLennan, A.
	2008	Association between apolipoprotein E genotype and cerebral palsy is not confirmed in a caucasian population	McMichael, G.; Gibson, C.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G.; MacLennan, A.
	2012	PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome	Heron, S.; Grinton, B.; Kivity, S.; Afawi, Z.; Zuberi, S.; Hughes, J.; Pridmore, C.; Hodgson, B.; Iona, X.; Sadleir, L.; Pelekanos, J.; Herlenius, E.; Goldberg-Stern, H.; Bassan, H.; Haan, E.; Korczyn, A.; Gardner, A.; Corbett, M.; Gecz, J.; Thomas, P.; et al.
	2006	The association between inherited cytokine polymorphisms and cerebral palsy	Gibson, C.; MacLennan, A.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G.; Hague, W.; Morton, M.
	2006	Associations between fetal inherited thrombophilia and adverse pregnancy outcomes	Gibson, C.; MacLennan, A.; Janssen, N.; Kist, W.; Hague, W.; Haan, E.; Goldwater, P.; Priest, K.; Dekker, G.
	1997	Mutation detection in FGFR2 craniosynostosis syndromes	Hollway, G.; Suthers, G.; Haan, E.; Thompson, E.; David, D.; Gecz, J.; Mulley, J.
	2005	Associations between inherited thrombophilias, gestational age, and cerebral palsy	Gibson, C.; MacLennan, A.; Hague, W.; Haan, E.; Priest, K.; Chan, A.; Dekker, G.