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Issue Date
Title
Author(s)
1995
Optimal polymerase chain reaction amplification for preimplantation diagnosis in cystic fibrosis (∆F508)
Cui, K.H.
;
Haan, E.
;
Wang, L.J.
;
Matthews, C.
1997
Perinatal risk factors for developmental dysplasia of the hip
Chan, A.
;
McCaul, K.
;
Cundy, P.
;
Haan, E.
;
Byron-Scott, R.
2009
A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology
Talseth-Palmer, B.
;
Bowden, N.
;
Meldrum, C.
;
Nicholl, J.
;
Thompson, E.
;
Friend, K.
;
Liebelt, J.
;
Bratkovic, D.
;
Haan, E.
;
Yu, S.
;
Scott, R.
2010
Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families
Hynes, K.
;
Tarpey, P.
;
Dibbens, L.
;
Bayly, M.
;
Berkovic, S.
;
Smith, R.
;
Al Raisi, Z.
;
Turner, S.
;
Brown, N.
;
Desai, T.
;
Haan, E.
;
Turner, G.
;
Christodoulou, J.
;
Leonard, H.
;
Gill, D.
;
Stratton, M.
;
Gecz, J.
;
Scheffer, I.
2009
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype
Spurlock, G.
;
Bennett, E.
;
Chuzhanova, N.
;
Thomas, N.
;
H-Ping, J.
;
Side, L.
;
Davies, S.
;
Haan, E.
;
Kerr, B.
;
Huson, S.
;
Upadhyaya, M.
2013
C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients
Dobson-Stone, C.
;
Hallupp, M.
;
Loy, C.
;
Thompson, E.
;
Haan, E.
;
Sue, C.
;
Panegyres, P.
;
Razquin, C.
;
Seijo-Martinez, M.
;
Ramon, R.
;
Gascon, J.
;
Campdelacreu, J.
;
Schmoll, B.
;
Volk, A.
;
Brooks, W.
;
Schofield, P.
;
Pastor, P.
;
Kwok, J.
;
Wider, C.
2013
In utero and early postnatal presentation of autoimmune lymphoproliferative syndrome in a family with a novel FAS mutation
Hansford, J.
;
Pal, M.
;
Poplawski, N.
;
Haan, E.
;
Boog, B.
;
Ferrante, A.
;
Davis, J.
;
Niemela, J.
;
Rao, V.
;
Suppiah, R.
2012
Cytomegalovirus and Epstein–Barr virus may be associated with some cases of cerebral palsy
McMichael, G.
;
MacLennan, A.
;
Gibson, C.
;
Alvino, E.
;
Goldwater, P.
;
Haan, E.
;
Dekker, G.
2014
FRA2A is a CGG repeat expansion associated with silencing of AFF3
Metsu, S.
;
Rooms, L.
;
Rainger, J.
;
Taylor, M.
;
Bengani, H.
;
Wilson, D.
;
Chilamakuri, C.
;
Morrison, H.
;
Vandeweyer, G.
;
Reyniers, E.
;
Douglas, E.
;
Thompson, G.
;
Haan, E.
;
Gecz, J.
;
FitzPatrick, D.
;
Kooy, R.
;
Pearson, C.
2006
Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource
Mann, G.
;
Thorne, H.
;
Balleine, R.
;
Butow, P.
;
Clarke, C.
;
Edkins, E.
;
Evans, G.
;
Fereday, S.
;
Haan, E.
;
Gattas, M.
;
Giles, G.
;
Goldblatt, J.
;
Hopper, J.
;
Kirk, J.
;
Leary, J.
;
Lindeman, G.
;
Niedermayr, E.
;
Phillips, K.
;
Picken, S.
;
Pupo, G.
;
et al.
Discover
Author
12
Gecz, J.
8
Ades, L.
8
Chan, A.
7
MacLennan, A.
6
Dekker, G.
6
et al.
5
Gibson, C.
5
Keane, R.
5
McMichael, G.
5
Sutherland, G.
.
next >
Subject
55
Female
44
Male
26
Adult
19
Child
17
Pregnancy
16
Pedigree
15
Syndrome
14
Abnormalities, Multiple
14
Child, Preschool
14
Mutation
.
next >
Date issued
18
2010 - 2016
26
2000 - 2009
28
1995 - 1999