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Cited2 haploinsufficiency is associated with congenital heart defects in mouse and man: Introducing the GO-CHD Study by Bentham, J, Bamforth, S, Braganca, J, Carballo, S, Michell, A, Bilski, M, Broadbent, C, Farthing, C, Franklyn, A, Schneider, J, Adwani, S, Devriendt, K, Keavney, B, Goodskip, J, Scambler, P, Watkins, H, Bhattacharya, S
Published 2006Conference item -
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VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5. by Szumska, D, Pieles, G, Essalmani, R, Bilski, M, Mesnard, D, Kaur, K, Franklyn, A, El Omari, K, Jefferis, J, Bentham, J, Taylor, J, Schneider, J, Arnold, S, Johnson, P, Tymowska-Lalanne, Z, Stammers, D, Clarke, K, Neubauer, S, Morris, A, Brown, S, Shaw-Smith, C, Cama, A, Capra, V, Ragoussis, J, Constam, D
Published 2008Journal article