HuGE Literature Finder
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Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot. Circulation research 2019 Feb 124 (4): 553-563. Page Donna J, Miossec Matthieu J, Williams Simon G, Monaghan Richard M, Fotiou Elisavet, Cordell Heather J, Sutcliffe Louise, Topf Ana, Bourgey Mathieu, Bourque Guillaume, Eveleigh Robert, Dunwoodie Sally L, Winlaw David S, Bhattacharya Shoumo, Breckpot Jeroen, Devriendt Koenraad, Gewillig Marc, Brook J David, Setchfield Kerry J, Bu'Lock Frances A, O'Sullivan John, Stuart Graham, Bezzina Connie R, Mulder Barbara J M, Postma Alex V, Bentham James R, Baron Martin, Bhaskar Sanjeev S, Black Graeme C, Newman William G, Hentges Kathryn E, Lathrop G Mark, Santibanez-Koref Mauro, Keavney Bernard |
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot. Nature genetics 2009 Aug 41 (8): 931-5. Greenway Steven C, Pereira Alexandre C, Lin Jennifer C, DePalma Steven R, Israel Samuel J, Mesquita Sonia M, Ergul Emel, Conta Jessie H, Korn Joshua M, McCarroll Steven A, Gorham Joshua M, Gabriel Stacey, Altshuler David M, Quintanilla-Dieck Maria de Lourdes, Artunduaga Maria Alexandra, Eavey Roland D, Plenge Robert M, Shadick Nancy A, Weinblatt Michael E, De Jager Philip L, Hafler David A, Breitbart Roger E, Seidman Jonathan G, Seidman Christine |
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