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Rare variants found in the 93 Tetralogy of Fallot patients.

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posted on 2014-08-05, 06:53 authored by Ana Töpf, Helen R. Griffin, Elise Glen, Rachel Soemedi, Danielle L. Brown, Darroch Hall, Thahira J. Rahman, Jyrki J. Eloranta, Christoph Jüngst, A. Graham Stuart, John O'Sullivan, Bernard D. Keavney, Judith A. Goodship

Inh  =  Inheritance: P = paternal, M = maternal. Frequency data is shown for the 500 ethnically matched controls studied and also NHLBI (Exome Sequencing Project) and 1000genomes data (European populations only). Data for the previously reported TBX1 variants is included.

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