Associated Papers
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly.
Kim A et al.
Brain : a Journal of Neurology, 2019
30508070 (PubMed )
Supplement: awy290_supplementary_table_s1.pdf
Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD.
Prokop JW et al.
Journal of the American Society of Nephrology : Jasn, 2018
Select a paper to view details