Adelaide Research & Scholarship
Browsing "Molecular and Biomedical Science publications" by Author Haan, E.
Showing results 1 to 7 of 7
Preview | Issue Date | Title | Author(s) |
| 2002 | A familial cryptic subtelomeric deletion 12p with variable phenotypic effect | Baker, E.; Hinton, L.; Callen, D.; Haan, E.; Dobbie, A.; Sutherland, G. |
| 2006 | Diagnosis of foetal alcohol syndrome and alcohol use in pregnancy: A survey of paediatricians' knowledge, attitudes and practice | Elliott, E.; Payne, J.; Haan, E.; Bower, C. |
| 2001 | Karyotypes found in the population declared at increased risk of Down Syndrome following maternal serum screening | Ryall, R.; Callen, D.; Cocciolone, R.; Duvnjak, A.; Esca, R.; Frantzis, N.; Gjerde, E.; Haan, E.; Hocking, T.; Sutherland, G.; Thomas, D.; Webb, F. |
| 2011 | Late-onset variant fibrodysplasia ossificans progressiva leading to misdiagnosis of ankylosing spondylitis | Barnett, C.; Dugar, M.; Haan, E. |
| 2000 | Universal periconceptional folate supplementation: chasing a dream? | Chan, A.; Haan, E. |
| 2009 | Upper limb orthoses and assistive technology utilization in children with hemiplegic cerebral palsy recruited from a population register | Russo, R.; Atkins, R.; Haan, E.; Crotty, M. |
| 2013 | Yunis-VarĂ³n Syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase | Campeau, P.; Lenk, G.; Lu, J.; Bae, Y.; Burrage, L.; Turnpenny, P.; Corona-Rivera, J.; Morandi, L.; Mora, M.; Reutter, H.; Vulto-van Silfhout, A.; Faivre, L.; Haan, E.; Gibbs, R.; Meisler, M.; Lee, B. |