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Results 1-10 of 91 (Search time: 0.002 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.
2007
Upper-limb botulinum toxin A injection and occupational therapy in children with hemiplegic cerebral palsy identified from a population register: A single-blind, randomized, controlled trial
Russo, R.
;
Crotty, M.
;
Miller, M.
;
Murchland, S.
;
Flett, P.
;
Haan, E.
1995
Maternal serum screening and prenatal diagnosis for birth defects
Suthers, G.
;
Haan, E.
2008
Combining first and second trimester markers for Down syndrome screening: Think twice
Cocciolone, R.
;
Brameld, K.
;
OLeary, P.
;
Haan, E.
;
Muller, P.
;
Shand, K.
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.
1999
Origins of accessory small ring marker chromosomes derived from chromosome 1
Callen, D.
;
Eyre, H.
;
Fang, Y.
;
Guan, X.
;
Veleba, A.
;
Martin, N.
;
McGill, J.
;
Haan, E.
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.
Discover
Author
13
Gecz, J.
12
Thompson, E.
9
Ades, L.
9
Chan, A.
9
et al.
6
Sutherland, G.
6
Suthers, G.
5
Butow, P.
5
Eyre, H.
5
Friend, K.
.
next >
Subject
13
Pregnancy
12
Base Sequence
12
Molecular Sequence Data
11
Infant
10
Adolescent
10
Intellectual Disability
9
Middle Aged
8
Infant, Newborn
8
South Australia
7
Chromosome Mapping
.
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Date issued
24
2010 - 2016
35
2000 - 2009
32
1995 - 1999