Associated Papers
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1013.391
Functionally significant, rare transcription factor variants in tetralogy of Fallot.
Töpf A et al.
Plos One, 2014
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