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Effect of prematurity on genome wide methylation in the placenta.
Sequencing of the IL6 gene in a case-control study of cerebral palsy in children.
Targeted 'next-generation' sequencing in anophthalmia and microphthalmia patients confirms SOX2, OTX2 and FOXE3 mutations.
Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type Ib.