Disease: Midline developmental field defects
- An evolutionary and developmental biology approach to gastroschisis
- Cell senescence in neuropathology: A focus on neurodegeneration and tumours
- Is VACTERL a laterality defect?
- Ivemark syndrome-a rare entity with specific anatomical features
- LRP2 is an auxiliary SHH receptor required to condition the forebrain ventral midline for inductive signals
- Membranous aplasia cutis congenita: A rare case report highlighting clinical presentation, genetic insights, and the need for comprehensive evaluation
- Optic nerve hypoplasia
- Oropharyngeal teratoma, oral duplication, cervical diplomyelia and anencephaly in a 22-week fetus: A review of the craniofacial teratoma syndrome
- Risk factors for nonsyndromic holoprosencephaly: a Manitoba case-control study
- Robo recruitment of the Wave regulatory complex plays an essential and conserved role in midline repulsion
- Role of Matrix Gla protein in midface development: Recent advances
- Spatiotemporally Controlled Mechanical Cues Drive Progenitor Mesenchymal-to-Epithelial Transition Enabling Proper Heart Formation and Function
- The Birth of the Eye Vesicle: When Fate Decision Equals Morphogenesis
- The VACTERL association: mosaic mitotic aneuploidy as a cause and a model
- Using whole mount in situ hybridization to link molecular and organismal biology
- Zebrafish con/disp1 reveals multiple spatiotemporal requirements for Hedgehog-signaling in craniofacial development