Showing 1 - 10 results of 10 for search 'Barnett, P', 查询时间: 0.05s
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TBX3 and its splice variant TBX3 + exon 2a are functionally similar. 由 Hoogaars, WM, Barnett, P, Rodriguez, M, Clout, D, Moorman, A, Goding, C, Christoffels, V
出版 2008Journal article -
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Cost-effectiveness of newer antiretroviral drugs in treatment-experienced patients with multidrug-resistant HIV disease. 由 Bayoumi, A, Barnett, P, Joyce, V, Griffin, S, Sun, H, Bansback, N, Holodniy, M, Sanders, G, Brown, S, Kyriakides, T, Angus, B, Cameron, D, Anis, A, Sculpher, M, Owens, D
出版 2013Journal article -
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T-box transcription factor 3 governs a transcriptional program for the function of the mouse atrioventricular conduction system 由 Mohan, RA, Bosada, FM, van Weerd, JH, van Duijvenboden, K, Wang, J, Mommersteeg, MTM, Hooijkaas, IB, Wakker, V, de Gier-de Vries, C, Coronel, R, Boink, GJJ, Bakkers, J, Barnett, P, Boukens, BJ, Christoffels, VM
出版 2020Journal article -
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Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. 由 Cordell, H, Bentham, J, Topf, A, Zelenika, D, Heath, S, Mamasoula, C, Cosgrove, C, Blue, G, Granados-Riveron, J, Setchfield, K, Thornborough, C, Breckpot, J, Soemedi, R, Martin, R, Rahman, T, Hall, D, van Engelen, K, Moorman, A, Zwinderman, A, Barnett, P, Koopmann, T, Adriaens, M, Varro, A, George, A, dos Remedios, C
出版 2013Journal article -
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Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 由 Cordell, H, Bentham, J, Topf, A, Zelenika, D, Heath, S, Mamasoula, C, Cosgrove, C, Blue, G, Granados-Riveron, J, Setchfield, K, Thornborough, C, Breckpot, J, Soemedi, R, Martin, R, Rahman, T, Hall, D, Van Engelen, K, Moorman, A, Zwinderman, A, Barnett, P, Koopmann, T, Adriaens, M, Varro, A, George, A, Dos Remedios, C
出版 2013Journal article