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Issue Date
Title
Author(s)
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.
1996
Characterisation of four novel fibrillin-1 mutations in the Marfan syndrome
Ades, L.
;
Haan, E.
;
Colley, A.
;
Richards, R.
2015
Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy
McMichael, G.
;
Bainbridge, M.
;
Haan, E.
;
Corbett, M.
;
Gardner, A.
;
Thompson, S.
;
Van Bon, B.
;
Van Eyk, C.
;
Broadbent, J.
;
Reynolds, C.
;
O'Callaghan, M.
;
Nguyen, L.
;
Adelson, D.
;
Russo, R.
;
Jhangiani, S.
;
Doddapaneni, H.
;
Muzny, D.
;
Gibbs, R.
;
Gecz, J.
;
MacLennan, A.
2002
Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies
Baker, E.
;
Hinton, L.
;
Callen, D.
;
Altree, M.
;
Dobbie, A.
;
Eyre, H.
;
Sutherland, G.
;
Thompson, E.
;
Thompson, P.
;
Woollatt, E.
;
Haan, E.
2013
RPGR mutations might cause reduced orientation of respiratory cilia
Bukowy-Blerytto, Z.
;
Zletkiewicz, E.
;
Loges, N.
;
Wittmer, M.
;
Geremek, M.
;
Olbrich, H.
;
Filegauf, M.
;
Voelkel, K.
;
Rutkiewicz, E.
;
Rutland, J.
;
Morgan, L.
;
Pogorzelski, A.
;
Martin, A.
;
Haan, E.
;
Berger, W.
;
Omran, H.
;
Witt, M.
2013
Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH
Nicholl, J.
;
Waters, W.
;
Suwalski, S.
;
Brown, S.
;
Hull, Y.
;
Harbord, M.
;
Entwistle, J.
;
Thompson, S.
;
Clark, D.
;
Pridmore, C.
;
Haan, E.
;
Barnett, C.
;
McGregor, L.
;
Liebelt, J.
;
Thompson, E.
;
Friend, K.
;
Bain, S.
;
Yu, S.
;
Mulley, J.
2006
FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited
Ades, L.
;
Sullivan, K.
;
Biggin, A.
;
Haan, E.
;
Brett, M.
;
Holman, K.
;
Dixon, J.
;
Robertson, S.
;
Holmes, A.
;
Rogers, J.
;
Bennetts, B.
2003
PEHO and PEHO-like syndromes: Report of five Australian cases
Field, M.
;
Grattan-Smith, P.
;
Piper, S.
;
Thompson, E.
;
Haan, E.
;
Edwards, M.
;
James, S.
;
Wilkinson, I.
;
Ades, L.
1995
Prenatal exposure to phenytoin, facial development and a possible role for vitamin K
Howe, A.
;
Lipson, A.
;
Sheffield, L.
;
Haan, E.
;
Halliday, J.
;
Jensen, F.
;
David, D.
;
Webster, W.
1995
Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome
Ades, L.
;
Morris, L.
;
Power, R.
;
Wilson, M.
;
Haan, E.
;
Bateman, J.
;
Milewicz, D.
;
Sillence, D.
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
64
Humans
50
Female
41
Male
25
Adult
18
Child
15
Pedigree
15
Syndrome
13
Abnormalities, Multiple
13
Child, Preschool
13
Mutation
.
next >
Date issued
24
2010 - 2016
35
2000 - 2009
32
1995 - 1999