Associated Papers
Pinpointing a potential role for CLEC12B in cancer predisposition through familial exome sequencing.
Derpoorter C et al.
Pediatric Blood & Cancer, 2019
Host genetic variants in sepsis risk: a field synopsis and meta-analysis.
Lu H et al.
Critical Care (london, England), 2019
30683156 (PubMed )
Supplement: 13054_2019_2313_MOESM1_ESM.docx
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1907.666
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