Items where Author is "Brook, J David"

Page, Donna J and Miossec, Matthieu J and Williams, Simon G and Monaghan, Richard M and Fotiou, Elisavet and Cordell, Heather and Sutcliffe, Louise and Topf, Ana and Bourgey, Mathieu and Bourque, Guillaume and Eveleigh, Robert and Dunwoodie, Sally L and Winlaw, David S and Bhattacharya, Shoumo and Breckpot, Jeroen and Devriendt, Koenraad and Gewillig, Marc and Brook, J David and Setchfield, Kerry Jane and Bu'Lock, Frances and O'sullivan, John J and Stuart, Graham and Bezzina, Connie R and Mulder, Barbara Jm and Postma, Alex V and Bentham, James R and Baron, Martin and Bhaskar, Sanjeev S and Black, Graeme C and Newman, William G and Hentges, Kathryn E and Lathrop, G Mark and Santibanez Koref, Mauro and Keavney, Bernard (2018) Whole Exome Sequencing Reveals the Major Genetic Contributors to Non-Syndromic Tetralogy of Fallot. Circulation Research, ePub. ISSN 1524-4571 (Not OA)

Granados-Riveron, Javier T and Pope, Mark and Bu'lock, Frances A and Thornborough, Christopher and Eason, Jacqueline and Setchfield, Kerry and Ketley, Ami and Kirk, Edwin P and Fatkin, Diane and Feneley, Michael P and Harvey, Richard P and Brook, J David (2012) Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations. Congenital heart disease, 7 (2). pp.151-9. ISSN 1747-0803 (PMC OA)