7 results on '"Hill, Matthew C."'
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2. Mutations in Hcfc1 and Ronin result in an inborn error of cobalamin metabolism and ribosomopathy
3. Identification of atrial fibrillation associated genes and functional non-coding variants
4. Tet inactivation disrupts YY1 binding and long-range chromatin interactions during embryonic heart development
5. SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
6. Endocrine lineage biases arise in temporally distinct endocrine progenitors during pancreatic morphogenesis
7. Development and rescue of human familial hypercholesterolaemia in a xenograft mouse model
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