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2. A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human. Issue 7 (6th March 2018)

5. Biallelic loss‐of‐function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome. Issue 4 (25th March 2018)

8. Emergent high fatality lung disease in systemic juvenile arthritis. Issue 12 (27th September 2019)