Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Tetralogy of Fallot and NOTCH1[original query] |
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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 |
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 |
Contribution of NOTCH1 genetic variants to bicuspid aortic valve and other congenital lesions. Heart (British Cardiac Society) 2022 3 108 (14): 1114-1120. Debiec Radoslaw Marek, Hamby Stephen E, Jones Peter D, Safwan Kassem, Sosin Michael, Hetherington Simon Lee, Sprigings David, Sharman David, Lee Kelvin, Salahshouri Pegah, Wheeldon Nigel, Chukwuemeka Andrew, Boutziouka Vasiliki, Elamin Mohamed, Coolman Sue, Asiani Manish, Kharodia Shireen, Skinner Gregory J, Samani Nilesh J, Webb Tom R, Bolger Aidan |
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