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Results 1-10 of 18 (Search time: 0.001 seconds).
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Issue Date
Title
Author(s)
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.
2000
New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndrome
Cox, T.
;
Allen, L.
;
Cox, L.
;
Hopwood, B.
;
Goodwin, B.
;
Haan, E.
;
Suthers, G.
2000
Intention to undergo prophylactic bilateral mastectomy in women at increased risk of developing hereditary breast cancer
Meiser, 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 Australia
Chan, A.
;
Pickering, J.
;
Haan, E.
;
Netting, M.
;
Burford, A.
;
Johnson, A.
;
Keane, R.
2002
The risk of mortality or cerebral palsy in twins: A collaborative population-based study
Scher, A.
;
Petterson, B.
;
Blair, E.
;
Ellenberg, J.
;
Grether, J.
;
Haan, E.
;
Reddihough, D.
;
Yeargin-Allsopp, M.
;
Nelson, K.
2001
Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome
Kelberman, D.
;
Tyson, J.
;
Chandler, D.
;
McInerney, A.
;
Slee, J.
;
Albert, D.
;
Aymat, A.
;
Botma, M.
;
Calvert, M.
;
Goldblatt, J.
;
Haan, E.
;
Laing, N.
;
Lim, J.
;
Malcolm, S.
;
Singer, S.
;
Winter, R.
;
Bitner-Glindzicz, M.
2000
Breast cancer screening uptake in women at increased risk of developing hereditary breast cancer
Meiser, B.
;
Butow, P.
;
Barratt, A.
;
Friedlander, M.
;
Kirk, J.
;
Gaff, C.
;
Haan, E.
;
Aittomaki, K.
;
Tucker, K.
2003
Disruption of the Serine/Threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation
Kalscheuer, V.
;
Tao, J.
;
Donnelly, A.
;
Hollway, G.
;
Schwinger, E.
;
Kubart, S.
;
Menzel, C.
;
Hoeltzenbein, M.
;
Tommerup, N.
;
Eyre, H.
;
Harbord, M.
;
Haan, E.
;
Sutherland, G.
;
Ropers, H.
;
Gecz, J.
2008
Pain characteristics and their association with quality of life and self-concept in children with hemiplegic cerebral palsy identified from a population register
Russo, R.
;
Miller, M.
;
Haan, E.
;
Cameron, I.
;
Crotty, M.
2009
Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2
Ghalamkarpour, A.
;
Debauche, C.
;
Haan, E.
;
Van Regemorter, N.
;
Snzajer, Y.
;
Thomas, D.
;
Revencu, N.
;
Gillerot, Y.
;
Boon, L.
;
Vikkula, M.
Discover
Author
3
Butow, P.
3
Chan, A.
3
Kirk, J.
2
Baker, E.
2
Crotty, M.
2
Eyre, H.
2
Friedlander, M.
2
Gattas, M.
2
Goldblatt, J.
2
Hinton, L.
.
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Subject
11
Adult
11
Male
7
Middle Aged
6
Adolescent
6
Child
5
Aged
5
Pregnancy
4
Abnormalities, Multiple
4
Health Knowledge, Attitudes, Prac...
4
Infant
.
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Date issued
3
2009
3
2008
1
2006
3
2005
1
2003
1
2002
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2001
4
2000