Associated Papers
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Huusko JM et al.
Plos Genetics, 2018
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1535.548
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