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Results 21-30 of 39 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
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.
2008
Genome analysis of the platypus reveals unique signatures of evolution
Warren, W.
;
Hillier, L.
;
Graves, J.
;
Birney, E.
;
Ponting, C.
;
Grutzner, F.
;
Belov, K.
;
Miller, W.
;
Clarke, L.
;
Chinwall, A.
;
Yang, S.
;
Heger, A.
;
Locke, D.
;
Miethke, P.
;
Waters, P.
;
Veyrunes, F.
;
Fulton, L.
;
Fulton, B.
;
Graves, T.
;
Wallis, J.
;
et al.
2009
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
Tarpey, P.
;
Smith, R.
;
Pleasance, E.
;
Whibley, A.
;
Edkins, S.
;
Hardy, C.
;
O'Meara, S.
;
Latimer, C.
;
Dicks, E.
;
Menzies, A.
;
Stephens, P.
;
Blow, M.
;
Greenman, C.
;
Xue, Y.
;
Tyler-Smith, C.
;
Thompson, D.
;
Gray, K.
;
Andrews, J.
;
Barthorpe, S.
;
Buck, G.
;
et al.
2008
Effect of 6-month calorie restriction and exercise on serum and liver lipids and markers of liver function
Larson-Meyer, D.
;
Newcomer, B.
;
Heilbronn, L.
;
Volaufova, J.
;
Smith, S.
;
Alfonso, A.
;
Lefevre, M.
;
Rood, J.
;
Williamson, D.
;
Ravussin, E.
;
DeLany, J.
;
de Jonge, L.
;
Nguyen, T.
;
Martin, C.
;
Most, M.
;
Greenway, F.
;
York-Crowe, E.
;
Anton, S.
;
Champagne, C.
;
Dahmer, B.
;
et al.
2008
Propafenone for the prevention of atrial tachyarrhythmias after cardiac surgery: a randomized, double-blind placebo-controlled trial
Morike, K.
;
Kivisto, K.
;
Schaeffeler, E.
;
Jagle, C.
;
Igel, S.
;
Drescher, S.
;
Fux, R.
;
Marx, C.
;
Hofmann, U.
;
Engel, C.
;
Wagner, F.
;
Delabar, U.
;
Meisner, C.
;
Bail, D.
;
Bohm, J.
;
Gleiter, C.
;
Ziemer, G.
;
Rein, J.
;
Hellberg, K.
;
Eichelbaum, M.
;
et al.
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.
2004
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation
Tarpey, P.
;
Parnau, J.
;
Blow, M.
;
Woffendin, H.
;
Bignell, G.
;
Cox, C.
;
Cox, J.
;
Davies, H.
;
Edkins, S.
;
Holden, S.
;
Korny, A.
;
Mallya, U.
;
Moon, J.
;
O'Meara, S.
;
Parker, A.
;
Stephens, P.
;
Stevens, C.
;
Teague, J.
;
Donnelly, A.
;
Mangelsdorf, M.
;
et al.
2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation
Burdon, K.
;
McKay, J.
;
Sale, M.
;
Russell-Eggitt, I.
;
Mackey, D.
;
Wirth, G.
;
Elder, J.
;
Nicoll, A.
;
Clarke, M.
;
FitzGerald, L.
;
Stankovich, J.
;
Shaw, M.
;
Sharma, S.
;
Gajovic, S.
;
Gruss, P.
;
Ross, S.
;
Thomas, P.
;
Voss, A.
;
Thomas, T.
;
Gecz, J.
;
et al.
2007
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor
Ali, A.
;
Christie, P.
;
Grigorieva, I.
;
Harding, B.
;
Van Esch, H.
;
Ahmed, S.
;
Bitner-Glindzicz, M.
;
Blind, E.
;
Bloch, C.
;
Christin, P.
;
Clayton, P.
;
Gecz, J.
;
Gilbert-Dussardier, B.
;
Guillen-Navarro, E.
;
Hackett, A.
;
Halac, I.
;
Hendy, G.
;
Lalloo, F.
;
Mache, C.
;
Mughal, Z.
;
et al.
2008
Pulmonary-vein isolation for atrial fibrillation in patients with heart failure
Khan, M.
;
Jais, P.
;
Cummings, J.
;
Di Biase, L.
;
Sanders, P.
;
Martin, D.
;
Kautzner, J.
;
Hao, S.
;
Themistoclakis, S.
;
Fanelli, R.
;
Potenza, D.
;
Massaro, R.
;
Wazni, O.
;
Schweikert, R.
;
Saliba, W.
;
Wang, P.
;
Al-Ahmad, A.
;
Beheiry, S.
;
Santarelli, P.
;
Starling, R.
;
et al.
Discover
Author
8
Edkins, S.
8
Tarpey, P.
7
O'Meara, S.
6
Barthorpe, S.
6
Buck, G.
6
Stevens, C.
5
Cole, J.
5
Jones, D.
5
Smith, R.
5
Teague, J.
.
next >
Subject
38
Humans
34
Female
14
Middle Aged
13
Mutation
12
Pedigree
10
Mental Retardation, X-Linked
9
Adult
8
Adolescent
8
Aged
8
Molecular Sequence Data
.
next >
Date issued
4
2009
12
2008
11
2007
4
2006
1
2004
4
2003
2
2002
1
2001