Marijke E.P. van den Elzen

Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes

Stephen R.F. Twigg, Christian Babbs, Marijke E.P. van den Elzen et al. · Human Molecular Genetics · 2013 · 71 citations · Full text

Adults with congenital or acquired facial disfigurement: Impact of appearance on social functioning

Marijke E.P. van den Elzen, Sarah L. Versnel, Steven E.R. Hovius et al. · Journal of Cranio-Maxillofacial Surgery · 2012 · 70 citations

Facial Plastic, Social Impairment, Social Psychology +11

Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1

Marijke E.P. van den Elzen, Stephen R.F. Twigg, Jacqueline A.C. Goos et al. · European Journal of Human Genetics · 2013 · 51 citations · Full text

Pathogenic Mutation, Mendelian Disorder, Genetic Disorder +10

Long-term results after 40 years experience with treatment of rare facial clefts: Part 1-oblique and paramedian clefts

Sarah L. Versnel, Marijke E.P. van den Elzen, Eppo B. Wolvius et al. · Journal of Plastic Reconstructive & Aesthetic Surgery · 2011 · 27 citations

Ophthalmology, Rare Facial Clefts, Medicine +8

Long-term results after 40 years experience with treatment of rare facial clefts: Part 2 – symmetrical median clefts

Marijke E.P. van den Elzen, Sarah L. Versnel, Eppo B. Wolvius et al. · Journal of Plastic Reconstructive & Aesthetic Surgery · 2011 · 15 citations

Cleft Lip, Rare Facial Clefts, Craniofacial Anomalies +7