Items where Author is "Bezzina, Connie R"

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Article

Copier, Jaƫl S and Bootsma, Marianne and Ng, Chai A and Wilde, Arthur A M and Bertels, Robin A and Bikker, Hennie and Christiaans, Imke and van der Crabben, Saskia N and Hol, Janna A and Koopmann, Tamara T and Knijnenburg, Jeroen and Lommerse, Aafke A J and van der Smagt, Jasper J and Bezzina, Connie R and Vandenberg, Jamie I and Verkerk, Arie O and Barge-Schaapveld, Daniela Q C M and Lodder, Elisabeth M (2022) Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance. Human Molecular Genetics, 32 (7). pp.1072-1082. ISSN 0964-6906

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)

This list was generated on Sun Mar 3 04:40:07 2024 AEDT.