GRANADOS-RIVERON JT, POPE M, BU'LOCK FA, THORNBOROUGH C, EASON J, SETCHFIELD K, KETLEY A, KIRK EP, FATKIN D, FENELEY MP, HARVEY RP and BROOK JD, 2011. Combined Mutation Screening Of Nkx2-5, Gata4, And Tbx5 In Congenital Heart Disease: Multiple Heterozygosity And Novel Mutations. Congenital Heart Disease. (In Press.)
RIVERON, JTG, GHOSH, TK, POPE, M, EASON, J, BULOCK, F, THOMBOROUGH, C, KIRK, EP, FATKIN, D, FENELEY, MP, HARVEY, RP, ARMOUR, JAL and BROOK, JD, 2010. alpha,-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects In: British Human Genetics Conference. S76-S76
MATSSON, H, EASON, J, BOOKWALTER, C S, KLAR, J, GUSTAVSSON, P, SUNNEGÅRDH, J, ENELL, H, JONZON, A, VIKKULA, M, GUTIERREZ, I, GRANADOS-RIVERON, J, POPE M, BU’LOCK F, COX J: ROBINSON T E, SONG F, BROOK J D, MARSTON S and TRYBUS K M AND DAHL N, 2008. Alpha-cardiac actin mutations produce atrial septal defects. Human Molecular Genetics. 17(2), 256-65
BREEN M, LANGFORD CF, CARTER NP, HOLMES NG, DICKENS HF, THOMAS R, SUTER N, RYDER EJ, POPE M and BINNS MM, 1. Fish Mapping And Identification Of Canine Chromosomes. The Journal Of Heredity. 90(1), 27-30