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Issue Date
Title
Author(s)
2001
Reduced total plasma homocyst(e)ine in children and adolescents with type 1 diabetes
Wiltshire, E.
;
Thomas, D.
;
Baghurst, P.
;
Couper, J.
2007
Testing the 8-syndrome structure of the child behavior checklist in 30 societies
Ivanova, M.
;
Achenbach, T.
;
Dumenci, L.
;
Rescorla, L.
;
Almqvist, F.
;
Weintraub, S.
;
Bilenberg, N.
;
Bird, H.
;
Chen, W.
;
Dobrean, A.
;
Dopfner, M.
;
Erol, N.
;
Fombonne, E.
;
Fonseca, A.
;
Frigerio, A.
;
Grietens, H.
;
Hannesdottir, H.
;
Kanbayashi, Y.
;
Lambert, M.
;
Larsson, B.
;
et al.
2000
Breast cancer screening uptake in women at increased risk of developing hereditary breast cancer
Meiser, B.
;
Butow, P.
;
Barratt, A.
;
Friedlander, M.
;
Kirk, J.
;
Gaff, C.
;
Haan, E.
;
Aittomaki, K.
;
Tucker, K.
2007
The generalizability of the Youth Self-Report syndrome structure in 23 societies
Ivanova, M.
;
Achenbach, T.
;
Dumenci, L.
;
Bilenberg, N.
;
Broberg, A.
;
Dopfner, M.
;
Forns, M.
;
Kanbayashi, Y.
;
Leung, P.
;
Mulatu, M.
;
Oh, K.
;
Sawyer, M.
;
Steinhausen, H.
;
Metzke, C.
;
Zilber, N.
;
Verhulst, F.
;
Rescorla, L.
;
Almqvist, F.
;
Bird, H.
;
Dobrean, A.
;
et al.
2005
Sleep-disordered breathing in Prader-Willi syndrome and its association with neurobehavioral abnormalities
O'Donoghue, F.
;
Camfferman, D.
;
Kennedy, J.
;
Martin, A.
;
Couper, T.
;
Lack, L.
;
Lushington, K.
;
McEvoy, R.
2003
Identification of three novel SEDL mutations, including mutation in the rare, non-canonical splice site of exon 4
Shaw, M.
;
Brunetti-Pierre, N.
;
Kadasi, L.
;
Kovacova, V.
;
van Maldergem, L.
;
De Brasi, D.
;
Salerno, M.
;
Gecz, J.
2001
Long-term outcomes of genetic counseling in women at increased risk of developing hereditary breast cancer
Meiser, B.
;
Butow, P.
;
Barratt, A.
;
Schneiden, V.
;
Gattas, M.
;
Kirk, J.
;
Gaff, C.
;
Suthers, G.
;
Tucker, K.
2000
Quantative histomorphometric analysis of the human growth plate from birth to adolescence
Byers, S.
;
Moore, A.
;
Byard, R.
;
Fazzalari, N.
2007
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in Exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation
Upadyaya, M.
;
Huson, S.
;
Davies, M.
;
Thomas, N.
;
Chuzhanova, N.
;
Giovannini, S.
;
Evans, D.
;
Howard, E.
;
Kerr, B.
;
Kerr, B.
;
Consoli, C.
;
Side, L.
;
Adams, D.
;
Pierpont, M.
;
Hatchen, R.
;
Barnicoat, A.
;
Li, H.
;
Wallace, P.
;
Van Biervliet, J.
;
Stevenson, D.
;
et al.
2002
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation
Bienvenu, T.
;
Poirier, K.
;
Friocourt, G.
;
Bahi, N.
;
Beaumont, D.
;
Fauchereau, F.
;
Jeema, L.
;
Zemni, R.
;
Vinet, M.
;
Francis, F.
;
Couvert, P.
;
Gomot, M.
;
Moraine, C.
;
van Bokhoven, H.
;
Kalscheuer, V.
;
Frints, S.
;
Gecz, J.
;
Ohzaki, K.
;
Chaabouni, H.
;
Fryns, J.
;
et al.
Discover
Author
13
Hopwood, J.
12
Couper, J.
11
Sawyer, M.
8
Baghurst, P.
8
Davidson, G.
7
Haan, E.
7
Wiltshire, E.
6
et al.
6
Gold, M.
6
Harmatz, P.
.
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Subject
106
Humans
79
Child
78
Female
73
Male
51
Adult
44
Child, Preschool
31
Infant
24
Middle Aged
20
Australia
15
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.
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Date issued
12
2009
12
2008
13
2007
8
2006
13
2005
9
2004
12
2003
10
2002
10
2001
9
2000
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