The ambiguous role of NKX2-5 mutations in thyroid dysgenesis by Van Engelen, K, Mommersteeg, M, Baars, M, Lam, J, Ilgun, A, Van Trotsenburg, A, Smets, A, Christoffels, V, Mulder, B, Postma, A

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. by 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

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 by 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

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. by Cordell, H, Töpf, A, Mamasoula, C, Postma, A, Bentham, J, Zelenika, D, Heath, S, Blue, G, Cosgrove, C, Granados Riveron, J, Darlay, R, Soemedi, R, Wilson, I, Ayers, K, Rahman, T, Hall, D, Mulder, B, Zwinderman, A, van Engelen, K, Brook, J, Setchfield, K, Bu'Lock, F, Thornborough, C, O'Sullivan, J, Stuart, A