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Results 1-10 of 11 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2019
Genomic subtyping and therapeutic targeting of acute erythroleukemia
Iacobucci, I.
;
Wen, J.
;
Meggendorfer, M.
;
Choi, J.K.
;
Shi, L.
;
Pounds, S.B.
;
Carmichael, C.L.
;
Masih, K.E.
;
Morris, S.M.
;
Lindsley, R.C.
;
Janke, L.J.
;
Alexander, T.B.
;
Song, G.
;
Qu, C.
;
Li, Y.
;
Payne-Turner, D.
;
Tomizawa, D.
;
Kiyokawa, N.
;
Valentine, M.
;
Valentine, V.
;
et al.
2012
Induction of labor versus expectant management in women with preterm prelabor rupture of membranes between 34 and 37 weeks: a randomized controlled trial
van der Ham, D.
;
Vijgen, S.
;
Nijhuis, J.
;
van Beek, J.
;
Opmeer, B.
;
Mulder, A.
;
Moonen, R.
;
Groenewout, M.
;
van Pampus, M.
;
Mantel, G.
;
Bloemenkamp, K.
;
van Wijngaarden, W.
;
Sikkema, M.
;
Haak, M.
;
Pernet, P.
;
Porath, M.
;
Molkenboer, J.
;
Kuppens, S.
;
Kwee, A.
;
Kars, M.
;
et al.
;
Middleton, P.
2011
Association between common variation at the FTO locus and changes in body mass index from infancy to late childhood: the complex nature of genetic association through growth and development
Sovio, U.
;
Mook-Kanamori, D.
;
Warrington, N.
;
Lawrence, R.
;
Briollais, L.
;
Palmer, C.
;
Cecil, J.
;
Sandling, J.
;
Syvanen, A.
;
Kaakinen, M.
;
Beilin, L.
;
Millwood, I.
;
Bennett, A.
;
Laitneen, J.
;
Pouta, A.
;
Molitor, J.
;
Smith, G.
;
Ben-Shlomo, Y.
;
Jaddoe, V.
;
Palmer, L.
;
et al.
;
Gibson, G.
2013
Identification Of KLHL41 mutations implicates BTB-Kelch-Mediated Ubiquitination as an alternate pathway to myofibrillar disruption in nemaline myopathy
Gupta, V.
;
Ravenscroft, G.
;
Shaheen, R.
;
Todd, E.
;
Swanson, L.
;
Shiina, M.
;
Ogata, K.
;
Hsu, C.
;
Clarke, N.
;
Darras, B.
;
Farrar, M.
;
Hashem, A.
;
Manton, N.
;
Muntoni, F.
;
North, K.
;
Sandaradura, S.
;
Nishino, I.
;
Hayashi, Y.
;
Sewry, C.
;
Thompson, E.
;
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.
2012
Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature
Kazenwadel, J.
;
Secker, G.
;
Liu, Y.
;
Rosenfeld, J.
;
Wildin, R.
;
Cuellar-Rodriguez, J.
;
Hsu, A.
;
Dyack, S.
;
Fernandez, C.
;
Chong, C.
;
Babic, M.
;
Bardy, P.
;
Shimamura, A.
;
Zhang, M.
;
Walsh, T.
;
Holland, S.
;
Hickstein, D.
;
Horwitz, M.
;
Hahn, C.
;
Scott, H.
;
et al.
2012
A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010
Lim, S.
;
Vos, T.
;
Flaxman, A.
;
Danaei, G.
;
Shibuya, K.
;
Adair-Rohani, H.
;
AlMazroa, M.
;
Amann, M.
;
Anderson, H.
;
Andrews, K.
;
Aryee, M.
;
Atkinson, C.
;
Bacchus, L.
;
Bahalim, A.
;
Balakrishnan, K.
;
Balmes, J.
;
Barker-Collo, S.
;
Baxter, A.
;
Bell, M.
;
Blore, J.
;
et al.
2012
Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010
Murray, C.
;
Vos, T.
;
Lozano, R.
;
Naghavi, M.
;
Flaxman, A.
;
Michaud, C.
;
Ezzati, M.
;
Shibuya, K.
;
Salomon, J.
;
Abdalla, S.
;
Aboyans, V.
;
Abraham, J.
;
Ackerman, I.
;
Aggarwal, R.
;
Ahn, S.
;
Ali, M.
;
Alvarado, M.
;
Anderson, H.
;
Anderson, L.
;
Andrews, K.
;
et al.
2012
Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010
Vos, T.
;
Flaxman, A.
;
Naghavi, M.
;
Lozano, R.
;
Michaud, C.
;
Ezzati, M.
;
Shibuya, K.
;
Salomon, J.
;
Abdalla, S.
;
Aboyans, V.
;
Abraham, J.
;
Ackerman, I.
;
Aggarwal, R.
;
Ahn, S.
;
Ali, M.
;
Alvarado, M.
;
Anderson, H.
;
Anderson, L.
;
Andrews, K.
;
Atkinson, C.
;
et al.
2018
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder
Frints, S.G.M.
;
Ozanturk, A.
;
RodrÃguez Criado, G.
;
Grasshoff, U.
;
de Hoon, B.
;
Field, M.
;
Manouvrier-Hanu, S.
;
E Hickey, S.
;
Kammoun, M.
;
Gripp, K.W.
;
Bauer, C.
;
Schroeder, C.
;
Toutain, A.
;
Mihalic Mosher, T.
;
Kelly, B.J.
;
White, P.
;
Dufke, A.
;
Rentmeester, E.
;
Moon, S.
;
Koboldt, D.C.
;
et al.
Discover
Author
4
Vos, T.
3
Anderson, H.
3
Andrews, K.
3
Flaxman, A.
3
Shibuya, K.
2
Abdalla, S.
2
Aboyans, V.
2
Abraham, J.
2
Ackerman, I.
2
Aggarwal, R.
.
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Subject
6
Middle Aged
4
Aged
4
Aged, 80 and over
4
Global Health
4
Mutation
3
Age Factors
3
Animals
3
Prevalence
3
Quality-Adjusted Life Years
3
Sex Factors
.
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