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Results 1-10 of 64 (Search time: 0.004 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.
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.
1998
A population-based study of abdominal wall defects in South Australia and Western Australia
Byron-Scott, R.
;
Haan, E.
;
Chan, A.
;
Bower, C.
;
Scott, H.
;
Clark, K.
1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
Muenke, M.
;
Gripp, K.
;
McDonald-McGinn, D.
;
Gaudenz, K.
;
Whitaker, L.
;
Bartlett, S.
;
Markowitz, R.
;
Robin, N.
;
Nwokoro, N.
;
Mulvihill, J.
;
Losken, H.
;
Mulliken, J.
;
Guttmacher, A.
;
Wilroy, R.
;
Clarke, L.
;
Hollway, G.
;
Ades, L.
;
Haan, E.
;
Mulley, J.
;
Cohen, M.
;
et al.
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.
1998
A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy.
Donnelly, A.
;
Haan, E.
;
Manson, J.
;
Mulley, J.
1997
High resolution characterisation of an interstitial deletion of less than 1.9Mb at 4p16.3 associated with Wolf-Hirschhorn Syndrome
Fang, Y.
;
Bain, S.
;
Haan, E.
;
Eyre, H.
;
MacDonald, M.
;
Wright, T.
;
Altherr, M.
;
Riess, O.
;
Sutherland, G.
;
Callen, D.
2012
Reproductive technologies and the risk of birth defects: The Authors reply
Davies, M.
;
Moore, V.
;
Haan, E.
1999
Homozygotes for FRA16B are normal
Hocking, T.
;
Feichtinger, W.
;
Schmid, M.
;
Haan, E.
;
Baker, E.
;
Sutherland, G.
Discover
Author
10
Chan, A.
9
Gecz, J.
6
Mulley, J.
6
Sutherland, G.
5
Ades, L.
5
et al.
5
Keane, R.
5
Thompson, E.
4
Baker, E.
4
Byron-Scott, R.
.
next >
Subject
64
Humans
42
Male
27
Adult
19
Pregnancy
16
Child
14
Pedigree
13
Syndrome
12
Infant, Newborn
12
Mutation
11
Abnormalities, Multiple
.
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Date issued
15
2010 - 2017
24
2000 - 2009
25
1995 - 1999