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Adelaide Research & Scholarship
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Results 111-115 of 115 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
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.
2012
Reproductive technologies and the risk of birth defects
Davies, M.
;
Moore, V.
;
Willson, K.
;
Van Essen, P.
;
Priest, K.
;
Scott, H.
;
Haan, E.
;
Chan, A.
1996
Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome: implications for mapping and cloning the BOR gene
Gu, J.
;
Wagner, M.
;
Haan, E.
;
Wells, D.
2000
Acampomelic campomelic dysplasia with SOX9 mutation
Thong, M.
;
Scherer, G.
;
Kozlowski, K.
;
Haan, E.
;
Morris, L.
Discover
Author
22
MacLennan, A.
19
Dekker, G.
19
Gibson, C.
15
Gecz, J.
14
Chan, A.
14
Goldwater, P.
14
Priest, K.
12
McMichael, G.
12
Thompson, E.
9
Ades, L.
.
next >
Subject
72
Humans
55
Female
44
Male
26
Adult
19
Child
17
Pregnancy
16
Pedigree
15
Syndrome
14
Abnormalities, Multiple
14
Child, Preschool
.
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Date issued
36
2010 - 2016
47
2000 - 2009
32
1995 - 1999