Showing results 39 to 58 of 144
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| Preview | Issue Date | Title | Author(s) |
| 1998 | Effect of Parity, Gravidity, Previous Miscarriage, and Age On Risk of Downs-Syndrome - Population Based Study | Chan, A.; McCaul, K.; Keane, R.; Haan, E. |
| 2011 | Epidemiologic associations with cerebral palsy | O'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Goldwater, P.; Dekker, G. |
| 2010 | Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families | Hynes, K.; Tarpey, P.; Dibbens, L.; Bayly, M.; Berkovic, S.; Smith, R.; Al Raisi, Z.; Turner, S.; Brown, N.; Desai, T.; Haan, E.; Turner, G.; Christodoulou, J.; Leonard, H.; Gill, D.; Stratton, M.; Gecz, J.; Scheffer, I. |
| 2008 | Epilepsy and mental retardation limited to females: an under-recognized disorder | Scheffer, I.; Turner, S.; Dibbens, L.; Bayly, M.; Friend, K.; Hodgson, B.; Burrows, L.; Shaw, M.; Wei, C.; Ullmann, R.; Ropers, H.; Szepetowski, P.; Haan, E.; Mazarib, A.; Afawi, Z.; Neufeld, M.; Andrews, P.; Wallace, G.; Kivity, S.; Lev, D.; et al. |
| 2013 | Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH | Nicholl, J.; Waters, W.; Suwalski, S.; Brown, S.; Hull, Y.; Harbord, M.; Entwistle, J.; Thompson, S.; Clark, D.; Pridmore, C.; Haan, E.; Barnett, C.; McGregor, L.; Liebelt, J.; Thompson, E.; Friend, K.; Bain, S.; Yu, S.; Mulley, J. |
| 2005 | Familial Parry-Romberg disease | Anderson, P.; Molony, D.; Haan, E.; David, D. |
| 2006 | FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited | Ades, L.; Sullivan, K.; Biggin, A.; Haan, E.; Brett, M.; Holman, K.; Dixon, J.; Robertson, S.; Holmes, A.; Rogers, J.; Bennetts, B. |
| 2008 | Fetal alcohol syndrome: a prospective national surveillance study | Elliott, E.; Payne, J.; Morris, A.; Haan, E.; Bower, C. |
| 2012 | Fetal and maternal candidate single nucleotide polymorphism associations with Cerebral Palsy: a case-control study | O'Callaghan, M.; MacLennan, A.; Gibson, C.; McMichael, G.; Haan, E.; Broadbent, J.; Goldwater, P.; Painter, J.; Montgomery, G.; Dekker, G. |
| 2008 | Fetal exposure to herpesviruses may be associated with pregnancy-induced hypertensive disorders and preterm birth in a Caucasian population | Gibson, C.; Goldwater, P.; MacLennan, A.; Haan, E.; Priest, K.; Dekker, G. |
| 2011 | Fetal MBL2 haplotypes combined with viral exposure are associated with adverse pregnancy outcomes | Gibson, C.; MacLennan, A.; Haan, E.; Priest, K.; Dekker, G. |
| 1997 | First-trimester diagnosis of Smith-Lemli-Opitz syndrome | Sharp, P.; Haan, E.; Fletcher, J.; Khong, T.; Carey, W. |
| 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 | Folate awareness and the prevalence of neural tube defects in South Australia, 1966-2007 | Chan, A.; van Essen, P.; Scott, H.; Haan, E.; Sage, L.; Scott, J.; Gill, T.; Nguyen, A. |
| 2001 | "Folate before pregnancy": the impact on women and health professionals of a population-based health promotion campaign in South Australia | Chan, A.; Pickering, J.; Haan, E.; Netting, M.; Burford, A.; Johnson, A.; Keane, R. |
| 2014 | FRA2A is a CGG repeat expansion associated with silencing of AFF3 | Metsu, S.; Rooms, L.; Rainger, J.; Taylor, M.; Bengani, H.; Wilson, D.; Chilamakuri, C.; Morrison, H.; Vandeweyer, G.; Reyniers, E.; Douglas, E.; Thompson, G.; Haan, E.; Gecz, J.; FitzPatrick, D.; Kooy, R.; Pearson, C. |
| 1995 | FRAXE and mental retardation | Mulley, 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. |
| 2005 | Frequency of truly cryptic subtelomere abnormalities - a study of 534 patients and literature review | Yu, S.; Baker, E.; Hinton, L.; Eyre, H.; Waters, W.; Higgins, S.; Sutherland, G.; Haan, E. |
| 2014 | Frontotemporal dementia and its subtypes: a genome-wide association study | Ferrari, R.; Hernandez, D.; Nalls, M.; Rohrer, J.; Ramasamy, A.; Kwok, J.; Dobson-Stone, C.; Brooks, W.; Schofield, P.; Halliday, G.; Hodges, J.; Piguet, O.; Bartley, L.; Thompson, E.; Haan, E.; Hernández, I.; Ruiz, A.; Boada, M.; Borroni, B.; Padovani, A.; et al. |
| 1996 | Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470) | Gedeon, A.; Haan, E.; Mulley, J. |
