Esther Gill

Cell signaling and transcriptional regulation of osteoblast lineage commitment, differentiation, bone formation, and homeostasis

Whole genome sequencing in clinical practice

Recessive DEAF1 mutation associates with autism, intellectual disability, basal ganglia dysfunction and epilepsy

POMK mutation in a family with congenital muscular dystrophy with merosin deficiency, hypomyelination, mild hearing deficit and intellectual disability