1. Adelaide Research & Scholarship

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Results 21-30 of 31 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Localization of craniosynostosis Adelaide type to 4p16Hollway, G.; Phillips, H.; Ades, L.; Haan, E.; Muley, J.
1995A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyLaing, N.; Wilton, S.; Akkari, P.; Dorosz, S.; Boundy, K.; Kneebone, C.; Blumbergs, P.; White, S.; Watkins, H.; Love, D.; Haan, E.
1998Preferential pre-mRNA utilisation of an upstream cryptic 5' splice site created by a single base deletion mutation in exon 37 of the FBN-1 geneGibson, M.; Ellis, S.; Ades, L.; Haan, E.; Cleary, E.
1995Hydrometrocolpos and segmental colonic dilatation in a girl with megacystis-microcolon-intestinal hypoperistalsis syndromeDewan, P.; Brown, N.; Murthy, D.; Dnaga-Christian, B.; Haan, E.; Byard, R.; Watters, D.
1998The impact of rubella immunisation on the incidence of rubella, congenital rubella syndrome and rubella-related terminations of pregnancy in South AustraliaCheffins, T.; Chan, A.; Keane, R.; Haan, E.; Hall, R.
1998What constitutes cerebral palsy?Badawi, N.; Watson, L.; Petterson, B.; Blair, E.; Slee, J.; Haan, E.; Stanley, F.
1997Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomySmith, A.; Marks, R.; Haan, E.; Dixon, J.; Trent, R.
1995Optimal polymerase chain reaction amplification for preimplantation diagnosis in cystic fibrosis (∆F508)Cui, K.H.; Haan, E.; Wang, L.J.; Matthews, C.
1997Perinatal risk factors for developmental dysplasia of the hipChan, A.; McCaul, K.; Cundy, P.; Haan, E.; Byron-Scott, R.
1995FRAXE and mental retardationMulley, J.; Yu, S.; Loesch, D.; Hay, D.; Donnelly, A.; Gedeon, A.; Carbonell, P.; Lopez, I.; Glover, G.; Garbarron, I.; Yu, P.; Baker, E.; Haan, E.; Hockey, A.; Knight, S.; Daview, K.; Richards, R.; Sutherland, G.

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