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Results 1-10 of 21 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2005The prevalence of inherited thrombophilias in a Caucasian Australian populationGibson, C.; MacLennan, A.; Rudzki, Z.; Hague, W.; Haan, E.; Sharpe, P.; Priest, K.; Chan, A.; Dekker, G.; Khong, T.
2008Fetal exposure to herpesviruses may be associated with pregnancy-induced hypertensive disorders and preterm birth in a Caucasian populationGibson, C.; Goldwater, P.; MacLennan, A.; Haan, E.; Priest, K.; Dekker, G.
2009DNA from Buccal Swabs Suitable for High-Throughput SNP Multiplex AnalysisMcMichael, G.; Gibson, C.; O'Callaghan, M.; Goldwater, P.; Dekker, G.; Haan, E.; MacLennan, A.
2009The genomic basis of cerebral palsy: A HuGE systematic literature reviewO'Callaghan, M.; MacLennan, A.; Haan, E.; Dekker, G.
2013ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticityHirata, H.; McMichael, G.; Haan, E.; MacLennan, A.; Yap, T.; Nguyen, L.; Shaw, M.; Gecz, J.
2013Genetic and clinical contributions to cerebral palsy: A multi-variable analysisO'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Baghurst, P.; Goldwater, P.; Dekker, G.
2013Single-nucleotide polymorphism associations with preterm delivery: a case-control replication study and meta-analysisO'Callaghan, M.; MacLennan, A.; McMichael, G.; Haan, E.; Dekker, G.
2013Rare copy number variation in cerebral palsyMcMichael, 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.
2008Association between apolipoprotein E genotype and cerebral palsy is not confirmed in a caucasian populationMcMichael, G.; Gibson, C.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G.; MacLennan, A.
2006The association between inherited cytokine polymorphisms and cerebral palsyGibson, C.; MacLennan, A.; Goldwater, P.; Haan, E.; Priest, K.; Dekker, G.; Hague, W.; Morton, M.