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Results 1-10 of 11 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2008Folate awareness and the prevalence of neural tube defects in South Australia, 1966-2007Chan, A.; van Essen, P.; Scott, H.; Haan, E.; Sage, L.; Scott, J.; Gill, T.; Nguyen, A.
2000Intention to undergo prophylactic bilateral mastectomy in women at increased risk of developing hereditary breast cancerMeiser, B.; Butow, P.; Friedlander, M.; Schnieden, V.; Gattas, M.; Kirk, J.; Suthers, G.; Haan, E.; Tucker, K.
2001"Folate before pregnancy": the impact on women and health professionals of a population-based health promotion campaign in South AustraliaChan, A.; Pickering, J.; Haan, E.; Netting, M.; Burford, A.; Johnson, A.; Keane, R.
2002The risk of mortality or cerebral palsy in twins: A collaborative population-based studyScher, A.; Petterson, B.; Blair, E.; Ellenberg, J.; Grether, J.; Haan, E.; Reddihough, D.; Yeargin-Allsopp, M.; Nelson, K.
2000Breast cancer screening uptake in women at increased risk of developing hereditary breast cancerMeiser, B.; Butow, P.; Barratt, A.; Friedlander, M.; Kirk, J.; Gaff, C.; Haan, E.; Aittomaki, K.; Tucker, K.
2009Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2Ghalamkarpour, A.; Debauche, C.; Haan, E.; Van Regemorter, N.; Snzajer, Y.; Thomas, D.; Revencu, N.; Gillerot, Y.; Boon, L.; Vikkula, M.
2005Health professionals' knowledge, practice and opinions about fetal alcohol syndrome and alcohol consumption in pregnancyPayne, J.; Elliott, E.; D'Antoine, H.; O'Leary, C.; Mahony, A.; Haan, E.; Bower, C.
2005The Hunter-McAlpine syndrome results from duplication 5q35-qterHunter, A.; DuPont, B.; McLaughlin, M.; Hinton, L.; Baker, E.; Ades, L.; Haan, E.; Schwartz, C.
2000The impact of maternal serum screening on the birth prevalence of Down's syndrome and the use of amniocentesis and chorionic villus sampling in South AustraliaCheffins, T.; Chan, A.; Haan, E.; Ranieri, E.; Ryall, R.; Keane, R.; Byron-Scott, R.; Scott, H.; Gjerde, E.; Nguyen, A.; Ford, J.; Sykes, S.
2009SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotypeSpurlock, G.; Bennett, E.; Chuzhanova, N.; Thomas, N.; H-Ping, J.; Side, L.; Davies, S.; Haan, E.; Kerr, B.; Huson, S.; Upadhyaya, M.

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