Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1 by Van Den Elzen, M, Twigg, S, Goos, J, Hoogeboom, A, Van Den Ouweland, A, Wilkie, A, Mathijssen, I

Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1. by van den Elzen, M, Twigg, SR, Goos, J, Hoogeboom, A, van den Ouweland, A, Wilkie, A, Mathijssen, I

Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes. by Twigg, SR, Babbs, C, van den Elzen, M, Goriely, A, Taylor, S, McGowan, S, Giannoulatou, E, Lonie, L, Ragoussis, J, Sadighi Akha, E, Knight, S, Zechi-Ceide, R, Hoogeboom, J, Pober, B, Toriello, H, Wall, SA, Rita Passos-Bueno, M, Brunner, H, Mathijssen, I, Wilkie, A